A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983771



Internal ID20550811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71735655..71738345hg38UCSC Ensembl
chr10:73495412..73498102hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382691
hg192691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440042
Supporting Variants
Samples
Known GenesC10orf105, CDH23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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