A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027940



Internal ID19117158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113755816..113849664hg38UCSC Ensembl
Innerchr5:113091513..113185361hg19UCSC Ensembl
Innerchr5:113119412..113213260hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3893849
hg1993849
hg1893849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5784n100
Supporting Variantsnssv3647070, nssv3647069, nssv3647068
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)nsv1027940
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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