A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701524



Internal ID15438176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:46852728..46863975hg38UCSC Ensembl
Innerchr1:47318400..47329647hg19UCSC Ensembl
Innerchr1:47090987..47102234hg18UCSC Ensembl
Innerchr1:47030420..47041667hg17UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3811248
hg1911248
hg1811248
hg1711248
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525401
Supporting Variants
Samples
Known GenesCYP4Z2P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701524
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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