A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506515



Internal ID22564463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54445923..54452148hg38UCSC Ensembl
chr6:54310721..54316946hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg386226
hg196226
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845001
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506515
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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