A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606353



Internal ID20979424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104645434..104652074hg38UCSC Ensembl
chr7:104285881..104292521hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg386641
hg196641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221255
Samples
Known GenesLHFPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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