A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150999



Internal ID20718039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132943823..132944229hg38UCSC Ensembl
chr7:132628583..132628989hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422613
Supporting Variants
Samples
Known GenesCHCHD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0008


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