A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425145



Internal ID21082698
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 StatusM
Merged Variants
Supporting Variantsnssv18150971
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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