A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678288



Internal ID15414940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15262263..15267170hg38UCSC Ensembl
Innerchr1:15588759..15593666hg19UCSC Ensembl
Innerchr1:15461346..15466253hg18UCSC Ensembl
Innerchr1:15334065..15338972hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384908
hg194908
hg184908
hg174908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517234
Supporting Variants
Samples
Known GenesFHAD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678288
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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