A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155590



Internal ID20722630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26376001..26376500hg38UCSC Ensembl
chr7:26415621..26416120hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615639
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08524


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