A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669213



Internal ID15405865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:495722..518686hg38UCSC Ensembl
Innerchr19:495722..518686hg19UCSC Ensembl
Innerchr19:446722..469686hg18UCSC Ensembl
Innerchr19:446722..469686hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3822965
hg1922965
hg1822965
hg1722965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516566
Supporting Variants
Samples
Known GenesMADCAM1, TPGS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669213
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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