A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456132



Internal ID22514009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145603079..145622816hg38UCSC Ensembl
chr1:145812240..145831984hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3819738
hg1919745
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828100
Supporting Variants
Samples
Known GenesGPR89A, LOC100288142, LOC101929780, NBPF10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456132
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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