A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384512



Internal ID22442382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64200403..64202297hg38UCSC Ensembl
chr1:64666086..64667980hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381895
hg191895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872417
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384512
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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