A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580355



Internal ID16367764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56212123..56241523hg38UCSC Ensembl
Innerchr19:56723492..56752892hg19UCSC Ensembl
Innerchr19:61415304..61444704hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3829401
hg1929401
hg1829401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6583n54
Supporting Variantsnssv901821
Samples
Known GenesZSCAN5A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580355
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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