A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606059



Internal ID20979130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55504889..55563066hg38UCSC Ensembl
chr7:55572582..55630759hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3858178
hg1958178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227206
Samples
Known GenesVOPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606059
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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