A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569798



Internal ID18868079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20047351..20315817hg38UCSC Ensembl
Innerchr19:20158160..20426626hg19UCSC Ensembl
Innerchr19:20019160..20287626hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38268467
hg19268467
hg18268467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059188
Supporting Variants
Samples
Known GenesZNF486, ZNF90
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3569798
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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