A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607309



Internal ID6994243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157078357..157082145hg38UCSC Ensembl
Innerchr5:157078379..157082124hg38UCSC Ensembl
Outerchr5:157078336..157082167hg38UCSC Ensembl
chr5:156505368..156509156hg19UCSC Ensembl
Innerchr5:156505390..156509135hg19UCSC Ensembl
Outerchr5:156505347..156509178hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg383789
hg193789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12111023, essv12111024
SamplesHG03934, NA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607309
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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