A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118178



Internal ID18920597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77637242..77638642hg38UCSC Ensembl
Outerchr10:79397000..79398400hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980845
SamplesKWS1
Known GenesKCNMA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118178
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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