A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870623



Internal ID22645559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240590708..240591058hg38UCSC Ensembl
chr1:240754008..240754358hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364771
Samples
Known GenesGREM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870623
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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