A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468287



Internal ID22526176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224304974..224317159hg38UCSC Ensembl
chr1:224492676..224504861hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg3812186
hg1912186
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829459
Supporting Variants
Samples
Known GenesNVL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468287
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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