A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159463



Internal ID20726503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73666901..73668400hg38UCSC Ensembl
chr7:73081231..73082730hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608596
Supporting Variants
Samples
Known GenesVPS37D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159463
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03416


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