A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155622



Internal ID20722662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26854941..26855503hg38UCSC Ensembl
chr7:26894560..26895122hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601470
Supporting Variants
Samples
Known GenesSKAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00053


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