A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983113



Internal ID19221060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:123857542..123857650hg38UCSC Ensembl
Outerchr10:125617058..125617166hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145487
Supporting Variants
SamplesKWS1
Known GenesCPXM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983113
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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