A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451663



Internal ID22509535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171044990..171046294hg38UCSC Ensembl
chr1:171014131..171015435hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg381305
hg191305
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828539
Supporting Variants
Samples
Known GenesMROH9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451663
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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