A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017504



Internal ID19106721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:91797103..91883037hg38UCSC Ensembl
Innerchr5:91092920..91178854hg19UCSC Ensembl
Innerchr5:91128676..91214610hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3885935
hg1985935
hg1885935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639191
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)nsv1017504
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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