A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875916



Internal ID22650875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202955450..202955607hg38UCSC Ensembl
chr1:202924578..202924735hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359934
Samples
Known GenesADIPOR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875916
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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