A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121816



Internal ID18935412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:73873642..73874642hg38UCSC Ensembl
Outerchr10:75633400..75634400hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv479n106
Supporting Variantsnssv3968465
SamplesKWS2
Known GenesCAMK2G
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121816
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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