A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503685



Internal ID22561626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17523999..17526648hg38UCSC Ensembl
chr6:17524230..17526879hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382650
hg192650
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845159
Supporting Variants
Samples
Known GenesCAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503685
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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