A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415886



Internal ID21073439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149076302..149079804hg38UCSC Ensembl
chr7:148773394..148776896hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383503
hg193503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154005
Samples
Known GenesZNF786
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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