A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv989088



Internal ID16283044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2531805..2544396hg38UCSC Ensembl
Innerchr4:2533532..2546123hg19UCSC Ensembl
Innerchr4:2503330..2515921hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3812592
hg1912592
hg1812592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593420
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)nssv989088
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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