A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952524



Internal ID16954711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:20703762..20704661hg38UCSC Ensembl
Outerchr13:21277901..21278800hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998192
SamplesBILGI_BIOE
Known GenesIL17D
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952524
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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