A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923761



Internal ID22698988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71483760..71484965hg38UCSC Ensembl
chr10:73243517..73244722hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381206
hg191206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356789
Samples
Known GenesCDH23
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923761
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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