A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701330



Internal ID15091296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22068110..23033865hg38UCSC Ensembl
Innerchr19:22250912..23216667hg19UCSC Ensembl
Innerchr19:22042752..23008507hg18UCSC Ensembl
Innerchr19:22042752..23008507hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38965756
hg19965756
hg18965756
hg17965756
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525240
Supporting Variants
Samples
Known GenesLOC100996349, LOC440518, ZNF257, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701330
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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