A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024929



Internal ID19114147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181091753..181136849hg38UCSC Ensembl
Innerchr5:180518753..180563849hg19UCSC Ensembl
Innerchr5:180451359..180496455hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3845097
hg1945097
hg1845097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3650344, nssv3650343
Samples
Known GenesOR2V1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024929
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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