A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613636



Internal ID20986707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78382859..78406726hg38UCSC Ensembl
chr7:78012176..78036043hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3823868
hg1923868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158920
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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