A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134652



Internal ID20701692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104673733..104761237hg38UCSC Ensembl
chr6:105121608..105209112hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3887505
hg1987505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612233
Supporting Variants
Samples
Known GenesHACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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