A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653814



Internal ID15390466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25974297..25980992hg38UCSC Ensembl
Innerchr12:26127230..26133925hg19UCSC Ensembl
Innerchr12:26018497..26025192hg18UCSC Ensembl
Innerchr12:26018497..26025192hg17UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg386696
hg196696
hg186696
hg176696
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517117
Supporting Variants
Samples
Known GenesRASSF8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653814
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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