A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007900



Internal ID18750431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70093477..70217492hg38UCSC Ensembl
Innerchr4:70959194..71083209hg19UCSC Ensembl
Innerchr4:70993783..71117798hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38124016
hg19124016
hg18124016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5319n100
Supporting Variantsnssv3633071, nssv3633070
Samples
Known GenesC4orf40, CSN1S2BP, ODAM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007900
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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