A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471572



Internal ID21129125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93829880..93843870hg38UCSC Ensembl
chr12:94223656..94237646hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3813991
hg1913991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006244
Samples
Known GenesCRADD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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