A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976447



Internal ID19240172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:62603041..62608541hg38UCSC Ensembl
Outerchr10:64362800..64368300hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg385501
hg195501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115396
Supporting Variants
SamplesKWS2
Known GenesZNF365
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976447
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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