A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501555



Internal ID22559493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125702180..125707345hg38UCSC Ensembl
chr6:126023326..126028491hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg385166
hg195166
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844013
Supporting Variants
Samples
Known GenesLOC643623
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501555
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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