A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060440



Internal ID20627480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32231957..32237323hg38UCSC Ensembl
chr1:32697558..32702924hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg385367
hg195367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332663
Supporting Variants
Samples
Known GenesMTMR9LP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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