A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952519



Internal ID17301393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:18835761..18838060hg38UCSC Ensembl
Outerchr13:19409901..19412200hg19UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998186
SamplesBILGI_BIOE
Known GenesANKRD20A9P
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952519
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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