A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050977



Internal ID19140196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18471488..18690687hg38UCSC Ensembl
Innerchr13:19045628..19264827hg19UCSC Ensembl
Innerchr13:17943628..18162827hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38219200
hg19219200
hg18219200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1599n100
Supporting Variantsnssv3712705, nssv3526431, nssv3526432
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)nsv1050977
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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