A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617018



Internal ID20990089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12300711..12348221hg38UCSC Ensembl
chr7:12340337..12387847hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3847511
hg1947511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149426
Samples
Known GenesVWDE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617018
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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