A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156884



Internal ID20723924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20297012..20297795hg38UCSC Ensembl
chr7:20336635..20337418hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38784
hg19784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619072
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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