A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966676



Internal ID18898662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:12622901..12623501hg38UCSC Ensembl
Outerchr10:12664900..12665500hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112575
Supporting Variants
SamplesKWS2
Known GenesCAMK1D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966676
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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