A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869509



Internal ID22644444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205006274..205006431hg38UCSC Ensembl
chr1:204975402..204975559hg19UCSC 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 Variantsnssv17356968
Samples
Known GenesNFASC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869509
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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