A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983513



Internal ID20550553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6995754..7076303hg38UCSC Ensembl
chr10:7037716..7118265hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3880550
hg1980550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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