A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648136



Internal ID18599731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:138461691..138480010hg38UCSC Ensembl
Innerchr5:137797380..137815699hg19UCSC Ensembl
Innerchr5:137825279..137843598hg18UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3818320
hg1918320
hg1818320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017996
Supporting Variants
Samples
Known GenesEGR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3648136
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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