A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613115



Internal ID20986186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23740792..23744875hg38UCSC Ensembl
chr7:23780411..23784494hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384084
hg194084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154939
Samples
Known GenesSTK31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613115
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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