A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153632



Internal ID20720672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120180722..120185615hg38UCSC Ensembl
chr7:119820776..119825669hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg384894
hg194894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618803
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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