A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996837



Internal ID18840711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77041159..77041478hg38UCSC Ensembl
Outerchr10:78800917..78801236hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152231
Supporting Variants
SamplesKWB1
Known GenesKCNMA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996837
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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