A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150971



Internal ID20718011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132347614..132362757hg38UCSC Ensembl
chr7:132032373..132047516hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3815144
hg1915144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425145
Supporting Variants
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150971
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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