A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153153



Internal ID20720193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144842465..144847781hg38UCSC Ensembl
chr7:144539558..144544874hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385317
hg195317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419761
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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