A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695231



Internal ID15085197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161293590..161307811hg38UCSC Ensembl
Innerchr1:161263380..161277601hg19UCSC Ensembl
Innerchr1:159530004..159544225hg18UCSC Ensembl
Innerchr1:158076453..158090674hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3814222
hg1914222
hg1814222
hg1714222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517826
Supporting Variants
Samples
Known GenesMPZ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695231
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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