A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605740



Internal ID20978811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121392401..121400400hg38UCSC Ensembl
chr7:121032455..121040454hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227098
Samples
Known GenesFAM3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605740
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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