A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156758



Internal ID20723798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19520843..19573426hg38UCSC Ensembl
chr7:19560466..19613049hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3852584
hg1952584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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