A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874007



Internal ID22648957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118455760..118456035hg38UCSC Ensembl
chr1:118998383..118998658hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874007
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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