A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702562



Internal ID15439214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36624121..36653688hg38UCSC Ensembl
Innerchr2:36851264..36880831hg19UCSC Ensembl
Innerchr2:36704768..36734335hg18UCSC Ensembl
Innerchr2:36762915..36792482hg17UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3829568
hg1929568
hg1829568
hg1729568
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526283
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702562
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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