A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321637



Internal ID20854745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:246724001..246724400hg38UCSC Ensembl
chr1:246887303..246887702hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059867
Samples
Known GenesSCCPDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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