A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481607



Internal ID22539511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98232861..98240460hg38UCSC Ensembl
chr1:98698417..98706016hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830861
Supporting Variants
Samples
Known GenesLOC729987
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481607
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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