A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435575



Internal ID21093128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138102818..138105183hg38UCSC Ensembl
chr7:137787564..137789929hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382366
hg192366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155178
Samples
Known GenesAKR1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435575
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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