A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604674



Internal ID20977745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118065892..118088218hg38UCSC Ensembl
chr7:117705946..117728272hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3822327
hg1922327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233002
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604674
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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