A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325109



Internal ID20858239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92377164..92379981hg38UCSC Ensembl
chr1:92842721..92845538hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382818
hg192818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065179
Samples
Known GenesRPAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325109
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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