A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981659



Internal ID20548699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43561019..43569622hg38UCSC Ensembl
chr10:44056467..44065070hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388604
hg198604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455348
Supporting Variants
Samples
Known GenesZNF239
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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