A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695669



Internal ID15085635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15330878..15341628hg38UCSC Ensembl
Innerchr2:15471002..15481752hg19UCSC Ensembl
Innerchr2:15388453..15399203hg18UCSC Ensembl
Innerchr2:15421600..15432350hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3810751
hg1910751
hg1810751
hg1710751
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515567
Supporting Variants
Samples
Known GenesNBAS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695669
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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