A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617272



Internal ID20990343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115938879..115993137hg38UCSC Ensembl
chr7:115578933..115633191hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3854259
hg1954259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227663
Samples
Known GenesTFEC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617272
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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