A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006077



Internal ID19095295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33924776..33994140hg38UCSC Ensembl
Innerchr4:33926398..33995762hg19UCSC Ensembl
Innerchr4:33602793..33672157hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3869365
hg1969365
hg1869365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620652
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)nsv1006077
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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