A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982579



Internal ID18863786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:32024299..32024361hg38UCSC Ensembl
Outerchr10:32313227..32313289hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145437
Supporting Variants
SamplesKWS1
Known GenesKIF5B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982579
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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