A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146775



Internal ID19198104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69238359..69238673hg38UCSC Ensembl
Outerchr10:70998115..70998429hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995927
SamplesKWB1
Known GenesHKDC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146775
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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