A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874804



Internal ID22649758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202874551..202874628hg38UCSC Ensembl
chr1:202843679..202843756hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362632
Samples
Known GenesLOC148709
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874804
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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