A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432166



Internal ID21089719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137111137..137111962hg38UCSC Ensembl
chr7:136795884..136796709hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154435
Samples
Known GenesLOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432166
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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