A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695341



Internal ID15085307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15330878..15390017hg38UCSC Ensembl
Innerchr2:15471002..15530141hg19UCSC Ensembl
Innerchr2:15388453..15447592hg18UCSC Ensembl
Innerchr2:15421600..15480739hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3859140
hg1959140
hg1859140
hg1759140
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)nssv695341
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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