A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152361



Internal ID20719401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135519801..135533600hg38UCSC Ensembl
chr7:135204549..135218348hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3813800
hg1913800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152361
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00176


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