A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608494



Internal ID20981565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87648301..87650500hg38UCSC Ensembl
chr7:87277617..87279816hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161844
Samples
Known GenesABCB1, RUNDC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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