A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966692



Internal ID18885812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:63521140..63521940hg38UCSC Ensembl
Outerchr10:65280900..65281700hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112591
Supporting Variants
SamplesKWS2
Known GenesREEP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966692
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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