A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501773



Internal ID22559712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139162342..139165593hg38UCSC Ensembl
chr6:139483479..139486730hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg383252
hg193252
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844302
Supporting Variants
Samples
Known GenesHECA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501773
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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