A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611762



Internal ID20984833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2228509..2313419hg38UCSC Ensembl
chr7:2268144..2353054hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3884911
hg1984911
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217657
Samples
Known GenesFTSJ2, MAD1L1, MIR6836, NUDT1, SNX8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611762
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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