A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901975



Internal ID15849245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56407229..56561064hg38UCSC Ensembl
Innerchr19:56918598..57072433hg19UCSC Ensembl
Innerchr19:61610410..61764245hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38153836
hg19153836
hg18153836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580385
Supporting Variants
Samples
Known GenesZFP28, ZNF471, ZNF583, ZNF667, ZNF667-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901975
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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