A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139043



Internal ID338227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32232372..32246292hg38UCSC Ensembl
chr1:32697973..32711893hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3813921
hg1913921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903601
Samples
Known GenesMTMR9LP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139043
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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