A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321420



Internal ID20854525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26823279..26897389hg38UCSC Ensembl
chr1:27149770..27223880hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3874111
hg1974111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060615
Samples
Known GenesGPATCH3, GPN2, SFN, ZDHHC18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321420
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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