A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968250



Internal ID19235793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:130207137..130207511hg38UCSC Ensembl
Outerchr10:132005401..132005775hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113347
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968250
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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