A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491756



Internal ID21149309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124275377..124277438hg38UCSC Ensembl
chr12:124759923..124761984hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382062
hg192062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997265
Samples
Known GenesZNF664-FAM101A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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