A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161525



Internal ID20728565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94532801..94533600hg38UCSC Ensembl
chr7:94162113..94162912hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604510
Supporting Variants
Samples
Known GenesCASD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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