A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430941



Internal ID21088494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149108887..149112508hg38UCSC Ensembl
chr7:148805979..148809600hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383622
hg193622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154011
Samples
Known GenesZNF425
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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