A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026231



Internal ID19115448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:54646174..54686985hg38UCSC Ensembl
Innerchr5:53942003..53982814hg19UCSC Ensembl
Innerchr5:53977760..54018571hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3840812
hg1940812
hg1840812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5669n100
Supporting Variantsnssv3642136
Samples
Known GenesLOC102467080
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026231
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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