A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580386



Internal ID16021109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56413392..56561064hg38UCSC Ensembl
Innerchr19:56924761..57072433hg19UCSC Ensembl
Innerchr19:61616573..61764245hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38147673
hg19147673
hg18147673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6591n54
Supporting Variantsnssv901976, nssv901977
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)nsv580386
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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