A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702770



Internal ID15092736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41480992..41534847hg38UCSC Ensembl
Innerchr17:39637244..39691099hg19UCSC Ensembl
Innerchr17:36890770..36944625hg18UCSC Ensembl
Innerchr17:36890770..36944625hg17UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3853856
hg1953856
hg1853856
hg1753856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526466
Supporting Variants
Samples
Known GenesKRT13, KRT15, KRT19, KRT35, KRT36, MIR6510
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702770
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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