A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480081



Internal ID22537984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50342219..50377917hg38UCSC Ensembl
chr1:50807891..50843589hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3835699
hg1935699
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480081
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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