A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702027



Internal ID15438679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72579475..72613469hg38UCSC Ensembl
Innerchr1:73045158..73079152hg19UCSC Ensembl
Innerchr1:72817746..72851740hg18UCSC Ensembl
Innerchr1:72757179..72791173hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3833995
hg1933995
hg1833995
hg1733995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516582
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702027
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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