A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515728



Internal ID15442785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53396620..53510924hg38UCSC Ensembl
Innerchr19:53899873..54014178hg19UCSC Ensembl
Innerchr19:58591685..58705990hg18UCSC Ensembl
Innerchr19:58591685..58705990hg17UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38114305
hg19114306
hg18114306
hg17114306
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669801, nssv681432, nssv682372, nssv664595, nssv674634, nssv698698, nssv668424, nssv687446, nssv684216
Samples
Known GenesTPM3P9, ZNF761, ZNF765, ZNF813
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515728
Frequency
Sample Size2026
Observed Gain8
Observed Loss1
Observed Complex0
Frequencyn/a


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