A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609062



Internal ID20982133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:905578..987665hg38UCSC Ensembl
chr7:945215..1027301hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3882088
hg1982087
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231517
Samples
Known GenesADAP1, COX19, CYP2W1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609062
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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