A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998024



Internal ID18848233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:74569341..74572942hg38UCSC Ensembl
Outerchr10:76329099..76332700hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg383602
hg193602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152988
Supporting Variants
SamplesKWB1
Known GenesADK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998024
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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