A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872737



Internal ID22647678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40169320..40169642hg38UCSC Ensembl
chr1:40634992..40635314hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386322
Samples
Known GenesRLF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872737
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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