A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999810



Internal ID18840377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71496840..71496946hg38UCSC Ensembl
Outerchr10:73256597..73256703hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152630
Supporting Variants
SamplesKWB1
Known GenesCDH23
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999810
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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