A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608586



Internal ID20981657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2247809..2293323hg38UCSC Ensembl
chr7:2287444..2332958hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3845515
hg1945515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154248
Samples
Known GenesMIR6836, NUDT1, SNX8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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