A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330327



Internal ID20863484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84834609..84835204hg38UCSC Ensembl
chr1:85300292..85300887hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064776
Samples
Known GenesLPAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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