A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585313



Internal ID6625633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15594076..15610996hg38UCSC Ensembl
Innerchr1:15594576..15610496hg38UCSC Ensembl
Outerchr1:15593076..15611996hg38UCSC Ensembl
chr1:15920571..15937491hg19UCSC Ensembl
Innerchr1:15921071..15936991hg19UCSC Ensembl
Outerchr1:15919571..15938491hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3816921
hg1916921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9863648, essv9863647, essv9863650, essv9863652, essv9863651, essv9863649
SamplesHG02339, HG03298, HG02476, HG02549, NA19239, NA19834
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585313
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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