A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3646938



Internal ID18945219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106778097..106811381hg38UCSC Ensembl
Innerchr5:106113798..106147082hg19UCSC Ensembl
Innerchr5:106141697..106174981hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3833285
hg1933285
hg1833285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015781
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3646938
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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