A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326478



Internal ID20859613
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 StatusM
Merged Variants
Supporting Variantsnssv18060442
Samples
Known GenesMTMR9LP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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