A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522949



Internal ID15450242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170378583..170403091hg38UCSC Ensembl
Innerchr6:170687671..170712179hg19UCSC Ensembl
Innerchr6:170529596..170554104hg18UCSC Ensembl
Innerchr6:170605303..170629811hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3824509
hg1924509
hg1824509
hg1724509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698616
Samples
Known GenesFAM120B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522949
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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