A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332534



Internal ID20865706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70949079..71001278hg38UCSC Ensembl
chr1:71414762..71466961hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3852200
hg1952200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062840
Samples
Known GenesPTGER3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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