A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502450



Internal ID22560390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152756662..152763414hg38UCSC Ensembl
chr6:153077797..153084549hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg386753
hg196753
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844131
Supporting Variants
Samples
Known GenesVIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502450
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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