A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027667



Internal ID19116886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:118555864..118700883hg38UCSC Ensembl
Innerchr5:117891559..118036578hg19UCSC Ensembl
Innerchr5:117919458..118064477hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38145020
hg19145020
hg18145020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647229
Samples
Known GenesLOC101927280, LOC102467225
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027667
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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