A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417238



Internal ID21074791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137027931..137176815hg38UCSC Ensembl
chr7:136712678..136861562hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38148885
hg19148885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231515
Samples
Known GenesLOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417238
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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