A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477625



Internal ID21135178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120731901..120732500hg38UCSC Ensembl
chr12:121169704..121170303hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997695
Samples
Known GenesACADS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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