A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879326



Internal ID22654295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7585694..7588371hg38UCSC Ensembl
chr1:7645754..7648431hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382678
hg192678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373375
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879326
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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