A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769896



Internal ID18964945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77471041..77472542hg38UCSC Ensembl
chr10:79230799..79232300hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076366
Supporting Variants
SamplesKWP1
Known GenesKCNMA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769896
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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