A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952527



Internal ID17301401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:23945962..23955861hg38UCSC Ensembl
Outerchr13:24520101..24530000hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998195
SamplesBILGI_BIOE
Known GenesANKRD20A19P
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952527
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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