A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330014



Internal ID20863168
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 Variantsnssv18203599
Samples
Known GenesMTMR9LP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330014
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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