A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619831



Internal ID20992902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39606876..39610719hg38UCSC Ensembl
chr7:39646475..39650318hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg383844
hg193844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156800
Samples
Known GenesYAE1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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