A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157974



Internal ID20725014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66074569..66079110hg38UCSC Ensembl
chr7:65539556..65544097hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg384542
hg194542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614292
Supporting Variants
Samples
Known GenesASL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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