A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527551



Internal ID18825832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18485354..18745495hg38UCSC Ensembl
Innerchr13:19059494..19319635hg19UCSC Ensembl
Innerchr13:17957494..18217635hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38260142
hg19260142
hg18260142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044149
Supporting Variants
Samples
Known GenesLINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527551
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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