A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325544



Internal ID20858675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40086552..40087920hg38UCSC Ensembl
chr1:40552224..40553592hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg381369
hg191369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060732
Samples
Known GenesPPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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