A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701600



Internal ID15438252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44451741..44473966hg38UCSC Ensembl
Innerchr19:44955927..44978183hg19UCSC Ensembl
Innerchr19:49647767..49670023hg18UCSC Ensembl
Innerchr19:49647767..49670023hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3822226
hg1922257
hg1822257
hg1722257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525472
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701600
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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