A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970303



Internal ID18898056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:12200697..12200760hg38UCSC Ensembl
Outerchr10:12242696..12242759hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133971
Supporting Variants
SamplesKWS2
Known GenesCDC123
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970303
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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