A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427886



Internal ID21085439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140492401..140502700hg38UCSC Ensembl
chr7:140192201..140202500hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7133n223
Supporting Variantsnssv18150690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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