A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980716



Internal ID19222015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:81874944..81875444hg38UCSC Ensembl
Outerchr10:83634700..83635200hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143511
Supporting Variants
SamplesKWS1
Known GenesNRG3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980716
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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