A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606743



Internal ID20979814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102721201..102786600hg38UCSC Ensembl
chr7:102361648..102427047hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3865400
hg1965400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218894
Samples
Known GenesFAM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606743
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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