A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146975



Internal ID20714015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107580001..107580500hg38UCSC Ensembl
chr7:107220446..107220945hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602011
Supporting Variants
Samples
Known GenesBCAP29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.04964


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