A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612205



Internal ID20985276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106381616..106381893hg38UCSC Ensembl
chr7:106022062..106022339hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612205
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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