A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002051



Internal ID19091268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16333756..16362286hg38UCSC Ensembl
Innerchr4:16335379..16363909hg19UCSC Ensembl
Innerchr4:15944477..15973007hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3828531
hg1928531
hg1828531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5146n100
Supporting Variantsnssv3619844
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)nsv1002051
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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