A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3572094



Internal ID18523689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52815839..52883604hg38UCSC Ensembl
Innerchr19:53319092..53386857hg19UCSC Ensembl
Innerchr19:58010904..58078669hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3867766
hg1967766
hg1867766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060163
Supporting Variants
Samples
Known GenesZNF28, ZNF320, ZNF468
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3572094
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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