A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122536



Internal ID18903304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71496824..71496944hg38UCSC Ensembl
Outerchr10:73256581..73256701hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982624, nssv3968221
SamplesKWS1, KWS2
Known GenesCDH23
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122536
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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