A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970384



Internal ID18883013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:96887871..96887934hg38UCSC Ensembl
Outerchr10:98647628..98647691hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134045
Supporting Variants
SamplesKWS2
Known GenesLCOR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970384
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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