A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151234



Internal ID20718274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101935300..101940506hg38UCSC Ensembl
chr7:101578580..101583786hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385207
hg195207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602310
Supporting Variants
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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