A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100700



Internal ID20667740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46373988..46377248hg38UCSC Ensembl
chr3:46415479..46418739hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383261
hg193261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359791
Supporting Variants
Samples
Known GenesCCR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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