A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983122



Internal ID20550162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58077004..58078417hg38UCSC Ensembl
chr10:59836764..59838177hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381414
hg191414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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