A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445988



Internal ID22503858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63219923..63238995hg38UCSC Ensembl
chr6:63929828..63948900hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3819073
hg1919073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896144
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445988
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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