A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159535



Internal ID20726575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74395417..74396781hg38UCSC Ensembl
chr7:73809747..73811111hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381365
hg191365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613252
Supporting Variants
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159535
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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