A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440042



Internal ID21097595
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 StatusM
Merged Variants
Supporting Variantsnssv17983771
Samples
Known GenesC10orf105, CDH23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440042
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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