A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137250



Internal ID20704290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117615390..117621415hg38UCSC Ensembl
chr6:117936553..117942578hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg386026
hg196026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604352
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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