A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999100



Internal ID19158636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18940103..18973645hg38UCSC Ensembl
Innerchr4:18941726..18975268hg19UCSC Ensembl
Innerchr4:18550824..18584366hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3833543
hg1933543
hg1833543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5148n100
Supporting Variantsnssv3619873
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)nsv999100
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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