A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505806



Internal ID22563750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43487617..43495577hg38UCSC Ensembl
chr6:43455355..43463315hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg387961
hg197961
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845613
Supporting Variants
Samples
Known GenesTJAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505806
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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