A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655194



Internal ID15391846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151297100..151300476hg38UCSC Ensembl
Innerchr6:151618235..151621611hg19UCSC Ensembl
Innerchr6:151659928..151663304hg18UCSC Ensembl
Innerchr6:151710349..151713725hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383377
hg193377
hg183377
hg173377
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519279
Supporting Variants
Samples
Known GenesAKAP12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655194
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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