A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463802



Internal ID22521688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52575537..52587791hg38UCSC Ensembl
chr14:53042255..53054509hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3812255
hg1912255
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861057
Supporting Variants
Samples
Known GenesGPR137C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463802
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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