A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3640692



Internal ID18938973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:58643142..58664091hg38UCSC Ensembl
Innerchr5:57938969..57959918hg19UCSC Ensembl
Innerchr5:57974726..57995675hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3820950
hg1920950
hg1820950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020937
Supporting Variants
Samples
Known GenesRAB3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3640692
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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