A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959444



Internal ID18864609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77471042..77472542hg38UCSC Ensembl
Outerchr10:79230800..79232300hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381501
hg191501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110177
Supporting Variants
SamplesKWS1
Known GenesKCNMA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959444
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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