A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325438



Internal ID20858569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198699958..198701816hg38UCSC Ensembl
chr1:198669087..198670945hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg381859
hg191859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056803
Samples
Known GenesPTPRC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325438
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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