A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043433



Internal ID19132652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18471488..18652568hg38UCSC Ensembl
Innerchr13:19045628..19226708hg19UCSC Ensembl
Innerchr13:17943628..18124708hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38181081
hg19181081
hg18181081
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1598n100
Supporting Variantsnssv3526407, nssv3526408, nssv3712695, nssv3526409
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)nsv1043433
Frequency
Sample Size11257
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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