A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060442



Internal ID20627482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32236635..32246392hg38UCSC Ensembl
chr1:32702236..32711993hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg389758
hg199758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326478
Supporting Variants
Samples
Known GenesMTMR9LP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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