A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155553



Internal ID20722593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2576801..2578400hg38UCSC Ensembl
chr7:2616435..2618034hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602780
Supporting Variants
Samples
Known GenesIQCE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07978


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