A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615362



Internal ID7002251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146096204..146102037hg38UCSC Ensembl
Innerchr7:146096246..146101995hg38UCSC Ensembl
Outerchr7:146096162..146102079hg38UCSC Ensembl
chr7:145793297..145799129hg19UCSC Ensembl
Innerchr7:145793339..145799087hg19UCSC Ensembl
Outerchr7:145793255..145799171hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385834
hg195833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12997613, essv12997618, essv12997626, essv12997617, essv12997631, essv12997622, essv12997619, essv12997620, essv12997637, essv12997615, essv12997610, essv12997612, essv12997623, essv12997634, essv12997624, essv12997614, essv12997633, essv12997616, essv12997635, essv12997611, essv12997629, essv12997628, essv12997625, essv12997627, essv12997630, essv12997636, essv12997632, essv12997609, essv12997621
SamplesHG03121, HG02852, HG02836, NA19020, NA19819, NA19393, HG00737, NA19448, HG02840, HG02860, NA20291, NA19038, NA19024, NA19901, HG03073, HG01882, NA19461, HG02817, HG03388, HG02594, HG03539, HG02611, NA19360, HG03066, NA19351, HG02646, NA19213, NA18522, HG02629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615362
Frequency
Sample Size2504
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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