A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464442



Internal ID21121995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27013901..27014600hg38UCSC Ensembl
chr12:27166834..27167533hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000064
Samples
Known GenesTM7SF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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