A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457262



Internal ID21114815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85281201..85365400hg38UCSC Ensembl
chr12:85674979..85759178hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3884200
hg1984200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189531
Samples
Known GenesALX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457262
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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