A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978414



Internal ID20545454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1275926..1318167hg38UCSC Ensembl
chr10:1318121..1360362hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3842242
hg1942242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449099
Supporting Variants
Samples
Known GenesADARB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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