A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607782



Internal ID20980853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9554452..9694081hg38UCSC Ensembl
chr7:9594082..9733710hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38139630
hg19139629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162230
Samples
Known GenesPER4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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