A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598726



Internal ID6985861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174359273..174362865hg38UCSC Ensembl
Innerchr3:174359276..174362862hg38UCSC Ensembl
Outerchr3:174359270..174362868hg38UCSC Ensembl
chr3:174077063..174080655hg19UCSC Ensembl
Innerchr3:174077066..174080652hg19UCSC Ensembl
Outerchr3:174077060..174080658hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg383593
hg193593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11229656, essv11229659, essv11229671, essv11229648, essv11229669, essv11229670, essv11229644, essv11229655, essv11229658, essv11229662, essv11229645, essv11229650, essv11229668, essv11229663, essv11229646, essv11229664, essv11229643, essv11229660, essv11229666, essv11229672, essv11229651, essv11229652, essv11229665, essv11229653, essv11229654, essv11229674, essv11229661, essv11229647, essv11229657, essv11229667, essv11229673, essv11229649
SamplesHG02574, NA18507, HG02852, HG03455, HG02810, HG02588, HG02571, HG02882, NA19200, HG03048, HG02470, HG02878, HG01889, NA19449, HG03024, HG02256, NA18523, HG02568, HG02675, HG02813, HG02667, NA18909, NA19321, NA19147, HG02983, HG01915, NA20351, NA19223, HG03049, HG03538, HG02465, HG02643
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598726
Frequency
Sample Size2504
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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