A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402815



Internal ID21060368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43079348..43080244hg38UCSC Ensembl
chr6:43047086..43047982hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231016
Samples
Known GenesPTK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402815
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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