A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031609



Internal ID19120831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99986588..100111052hg38UCSC Ensembl
Innerchr5:99322292..99446756hg19UCSC Ensembl
Innerchr5:99350191..99474655hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38124465
hg19124465
hg18124465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5733n100
Supporting Variantsnssv3638084, nssv3638086, nssv3638085
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)nsv1031609
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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