A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521795



Internal ID15102402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151261497..151262834hg38UCSC Ensembl
Innerchr6:151582632..151583969hg19UCSC Ensembl
Innerchr6:151624325..151625662hg18UCSC Ensembl
Innerchr6:151674746..151676083hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381338
hg191338
hg181338
hg171338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694566
Samples
Known GenesAKAP12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521795
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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