A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417171



Internal ID21074724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135731586..135733369hg38UCSC Ensembl
chr7:135416334..135418117hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381784
hg191784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152380
Samples
Known GenesFAM180A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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