A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697949



Internal ID15087915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47373953..47421542hg38UCSC Ensembl
Innerchr19:47877210..47924799hg19UCSC Ensembl
Innerchr19:52569010..52616611hg18UCSC Ensembl
Innerchr19:52569010..52616611hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3847590
hg1947590
hg1847602
hg1747602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521341
Supporting Variants
Samples
Known GenesDHX34, MEIS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697949
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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