A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996093



Internal ID18846854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76495863..76501364hg38UCSC Ensembl
Outerchr10:78255621..78261122hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385502
hg195502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150621
Supporting Variants
SamplesKWB1
Known GenesC10orf11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996093
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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