A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615246



Internal ID20988317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87253014..87326798hg38UCSC Ensembl
chr7:86882330..86956114hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3873785
hg1973785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235544
Samples
Known GenesTP53TG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615246
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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