A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606171



Internal ID20979242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124783688..124798912hg38UCSC Ensembl
chr7:124423742..124438966hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3815225
hg1915225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218445
Samples
Known GenesLOC154872
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606171
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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