A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1005592



Internal ID16299548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:115007591..115008123hg38UCSC Ensembl
Innerchr4:115928747..115929279hg19UCSC Ensembl
Innerchr4:116148196..116148728hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38533
hg19533
hg18533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595229
Supporting Variants
Samples
Known GenesNDST4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1005592
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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