A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999114



Internal ID16945380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:65330463..65338962hg38UCSC Ensembl
Outerchr15:65622801..65631300hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951975
Supporting Variants
SamplesBILGI_BIOE
Known GenesIGDCC3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999114
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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