A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505762



Internal ID22563706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41036851..41040512hg38UCSC Ensembl
chr6:41004590..41008251hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg383662
hg193662
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844896
Supporting Variants
Samples
Known GenesUNC5CL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505762
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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