A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456264



Internal ID21113817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85020901..85021600hg38UCSC Ensembl
chr12:85414680..85415378hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38700
hg19699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004222
Samples
Known GenesTSPAN19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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