A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493055



Internal ID21150608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124911856..124913116hg38UCSC Ensembl
chr12:125396402..125397662hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381261
hg191261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997297
Samples
Known GenesUBC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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