A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519112



Internal ID15446405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31792051..31804447hg38UCSC Ensembl
Innerchr12:31944985..31957381hg19UCSC Ensembl
Innerchr12:31836252..31848648hg18UCSC Ensembl
Innerchr12:31836252..31848648hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3812397
hg1912397
hg1812397
hg1712397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696587
Samples
Known GenesH3F3C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519112
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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