A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616599



Internal ID20989670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26689227..26695474hg38UCSC Ensembl
chr7:26728846..26735093hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg386248
hg196248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155609
Samples
Known GenesSKAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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