A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608301



Internal ID20981372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114675721..114700474hg38UCSC Ensembl
chr7:114315776..114340529hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3824754
hg1924754
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234686
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608301
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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