A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020352



Internal ID18762887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111084170..111105496hg38UCSC Ensembl
Innerchr5:110419868..110441195hg19UCSC Ensembl
Innerchr5:110447767..110469094hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3821327
hg1921328
hg1821328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5781n100
Supporting Variantsnssv3647046
Samples
Known GenesWDR36
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020352
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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