A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426636



Internal ID21084189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132935413..132936000hg38UCSC Ensembl
chr7:132620173..132620760hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150997
Samples
Known GenesCHCHD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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