A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006140



Internal ID19095358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:81657253..82031845hg38UCSC Ensembl
Innerchr4:82578407..82952998hg19UCSC Ensembl
Innerchr4:82797431..83172022hg18UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38374593
hg19374592
hg18374592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633895, nssv3633897, nssv3633896
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)nsv1006140
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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