A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161697



Internal ID20728737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84150519..84152678hg38UCSC Ensembl
chr7:83779835..83781994hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382160
hg192160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618171
Supporting Variants
Samples
Known GenesSEMA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00044


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