A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611711



Internal ID20984782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122339716..122343243hg38UCSC Ensembl
chr7:121979770..121983297hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg383528
hg193528
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225591
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611711
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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