A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871746



Internal ID22646684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119470227..119471004hg38UCSC Ensembl
chr1:120012850..120013627hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871746
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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