A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871174



Internal ID22646111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105190796..105951622hg38UCSC Ensembl
chr1:105733418..106494244hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38760827
hg19760827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365182
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871174
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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