A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv996696



Internal ID16290652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42704111..42706471hg38UCSC Ensembl
Innerchr4:42706128..42708488hg19UCSC Ensembl
Innerchr4:42400885..42403245hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg382361
hg192361
hg182361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv996696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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