A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681432



Internal ID15071398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53431384..53510924hg38UCSC Ensembl
Innerchr19:53934637..54014178hg19UCSC Ensembl
Innerchr19:58626449..58705990hg18UCSC Ensembl
Innerchr19:58626449..58705990hg17UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3879541
hg1979542
hg1879542
hg1779542
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515728
Supporting Variants
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681432
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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