A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959596



Internal ID18872810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:77547249..77549149hg38UCSC Ensembl
Outerchr3:77596400..77598300hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118702
Supporting Variants
SamplesKWS1
Known GenesROBO2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959596
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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