A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456583



Internal ID22514461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23618273..23623006hg38UCSC Ensembl
chr1:23944763..23949496hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456583
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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