A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259947



Internal ID20469165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71483763..71484969hg38UCSC Ensembl
chr10:73243520..73244726hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747097
Supporting Variants
Samples
Known GenesCDH23
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259947
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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