A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155667



Internal ID20722707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2977519..2989968hg38UCSC Ensembl
chr7:3017153..3029602hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3812450
hg1912450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609015
Supporting Variants
Samples
Known GenesCARD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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