A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518962



Internal ID15446255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124077256..124098900hg38UCSC Ensembl
Innerchr12:124561803..124583446hg19UCSC Ensembl
Innerchr12:123127756..123149399hg18UCSC Ensembl
Innerchr12:123086683..123108326hg17UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3821645
hg1921644
hg1821644
hg1721644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696429
Samples
Known GenesZNF664-FAM101A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518962
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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