A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014580



Internal ID19103798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16338105..16362286hg38UCSC Ensembl
Innerchr4:16339728..16363909hg19UCSC Ensembl
Innerchr4:15948826..15973007hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3824182
hg1924182
hg1824182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5146n100
Supporting Variantsnssv3619859
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)nsv1014580
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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