A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036898



Internal ID19126117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18712716..18838135hg38UCSC Ensembl
Innerchr13:19286856..19412275hg19UCSC Ensembl
Innerchr13:18184856..18310275hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38125420
hg19125420
hg18125420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1605n100
Supporting Variantsnssv3714932
Samples
Known GenesANKRD20A9P, LINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036898
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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