A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694769



Internal ID15431421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30323255..30332678hg38UCSC Ensembl
Innerchr12:30476188..30485611hg19UCSC Ensembl
Innerchr12:30367455..30376878hg18UCSC Ensembl
Innerchr12:30367455..30376878hg17UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg389424
hg199424
hg189424
hg179424
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522000
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694769
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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