A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324521



Internal ID20857649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203073547..203075997hg38UCSC Ensembl
chr1:203042675..203045125hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382451
hg192451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056708
Samples
Known GenesPPFIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324521
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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