A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316774



Internal ID20849856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98989617..98993649hg38UCSC Ensembl
chr1:99455173..99459205hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg384033
hg194033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065964
Samples
Known GenesLPPR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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