A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157700



Internal ID20724740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52556009..52556774hg38UCSC Ensembl
chr7:52623705..52624470hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610771
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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