A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612277



Internal ID20985348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101084117..101093175hg38UCSC Ensembl
chr7:100727398..100736456hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg389059
hg199059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148384
Samples
Known GenesTRIM56
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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