A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605655



Internal ID20978726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:678620..789349hg38UCSC Ensembl
chr7:718257..828986hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38110730
hg19110730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158098
Samples
Known GenesHEATR2, PRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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