A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516582



Internal ID15443875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72555560..72618538hg38UCSC Ensembl
Innerchr1:73021243..73084221hg19UCSC Ensembl
Innerchr1:72793831..72856809hg18UCSC Ensembl
Innerchr1:72733264..72796242hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3862979
hg1962979
hg1862979
hg1762979
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705429, nssv677061, nssv669332, nssv672126, nssv702027
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516582
Frequency
Sample Size2026
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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