A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323759



Internal ID20856881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88835858..88836448hg38UCSC Ensembl
chr1:89301541..89302131hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064886
Samples
Known GenesPKN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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