A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372414



Internal ID22598083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:80783641..80787178hg38UCSC Ensembl
chr1:81249326..81252863hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg383538
hg193538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372414
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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