A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606782



Internal ID20979853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90315901..90343900hg38UCSC Ensembl
chr7:89945215..89973214hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3828000
hg1928000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232457
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606782
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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