A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457776



Internal ID22515657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227455773..227457572hg38UCSC Ensembl
chr1:227643474..227645273hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457776
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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