A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982809



Internal ID20549849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6285099..6286114hg38UCSC Ensembl
chr10:6327062..6328077hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447559
Supporting Variants
Samples
Known GenesLOC399715
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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