A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982687



Internal ID20549727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60287291..60287716hg38UCSC Ensembl
chr10:62047049..62047474hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454378
Supporting Variants
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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