A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979931



Internal ID20546971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37770436..37780330hg38UCSC Ensembl
chr10:38059364..38069258hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg389895
hg199895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450051
Supporting Variants
Samples
Known GenesZNF248
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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