A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv989318



Internal ID16283274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6301627..6303151hg38UCSC Ensembl
Innerchr4:6303354..6304878hg19UCSC Ensembl
Innerchr4:6354255..6355779hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381525
hg191525
hg181525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593498
Supporting Variants
Samples
Known GenesWFS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv989318
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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