A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596270



Internal ID16383679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177970257..178192956hg38UCSC Ensembl
Innerchr4:178891411..179114110hg19UCSC Ensembl
Innerchr4:179128405..179351104hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38222700
hg19222700
hg18222700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017037
Samples
Known GenesLINC01098
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596270
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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