A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146695



Internal ID18854726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48709156..48709428hg38UCSC Ensembl
Outerchr10:49917201..49917473hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995847
SamplesKWB1
Known GenesWDFY4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146695
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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