A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137935



Internal ID18908908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71760138..71760196hg38UCSC Ensembl
Outerchr10:73519895..73519953hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982625, nssv3970745
SamplesKWS1, KWS2
Known GenesC10orf54, CDH23
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137935
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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