A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076366



Internal ID18975730
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 StatusM
Merged Variants
Supporting Variantsnssv3769896
SamplesKWP1
Known GenesKCNMA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076366
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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