A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580356



Internal ID16367765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56212123..56251411hg38UCSC Ensembl
Innerchr19:56723492..56762780hg19UCSC Ensembl
Innerchr19:61415304..61454592hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3839289
hg1939289
hg1839289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6583n54
Supporting Variantsnssv901822
Samples
Known GenesZSCAN5A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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