A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605534



Internal ID20978605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103294154..103307159hg38UCSC Ensembl
chr7:102934601..102947606hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3813006
hg1913006
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225688
Samples
Known GenesPMPCB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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