A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870365



Internal ID22645301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8968979..8969275hg38UCSC Ensembl
chr1:9029038..9029334hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393741
Samples
Known GenesCA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870365
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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