A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016525



Internal ID19105744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:162911493..163081400hg38UCSC Ensembl
Innerchr4:163832645..164002552hg19UCSC Ensembl
Innerchr4:164052095..164222002hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38169908
hg19169908
hg18169908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634153
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)nsv1016525
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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