A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044769



Internal ID19133988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55672575..55741910hg38UCSC Ensembl
Innerchr13:56246710..56316044hg19UCSC Ensembl
Innerchr13:55144711..55214045hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3869336
hg1969335
hg1869335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523869
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)nsv1044769
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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