A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501825



Internal ID22559764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142208934..142214090hg38UCSC Ensembl
chr6:142530071..142535227hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg385157
hg195157
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844723
Supporting Variants
Samples
Known GenesVTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501825
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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