A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578500



Internal ID16019223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7067762..7127082hg38UCSC Ensembl
Innerchr19:7067773..7127093hg19UCSC Ensembl
Innerchr19:7018773..7078093hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3859321
hg1959321
hg1859321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893234
Samples
Known GenesINSR, ZNF557
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578500
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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