A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984704



Internal ID20551744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90811351..90811932hg38UCSC Ensembl
chr10:92571108..92571689hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438315
Supporting Variants
Samples
Known GenesHTR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0049


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