A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152392



Internal ID20719432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135900337..135902440hg38UCSC Ensembl
chr7:135585085..135587188hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382104
hg192104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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