A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001740



Internal ID19090957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:31847601..32765759hg38UCSC Ensembl
Innerchr4:31849223..32767381hg19UCSC Ensembl
Innerchr4:31493121..32411279hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38918159
hg19918159
hg18918159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620640
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001740
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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