A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154048



Internal ID20721088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149645118..149646877hg38UCSC Ensembl
chr7:149342209..149343968hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381760
hg191760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154048
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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