A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046754



Internal ID19135973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57373019..57421567hg38UCSC Ensembl
Innerchr13:57947153..57995701hg19UCSC Ensembl
Innerchr13:56845154..56893702hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3848549
hg1948549
hg1848549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526569
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)nsv1046754
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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