A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328224



Internal ID20861369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98968313..98968911hg38UCSC Ensembl
chr1:99433869..99434467hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065957
Samples
Known GenesLPPR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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