A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137893



Internal ID18908915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:32024196..32024258hg38UCSC Ensembl
Outerchr10:32313124..32313186hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985439, nssv3990413
SamplesKWS2, KWS1
Known GenesKIF5B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137893
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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