A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955927



Internal ID16958114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77041136..77041423hg38UCSC Ensembl
Outerchr10:78800894..78801181hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003526
SamplesBILGI_BIOE
Known GenesKCNMA1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955927
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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