A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966687



Internal ID18881909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:47438562..47461362hg38UCSC Ensembl
Outerchr10:48278000..48300800hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3822801
hg1922801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112586
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966687
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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