A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619730



Internal ID20992801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67113285..67123518hg38UCSC Ensembl
chr7:66578272..66588505hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3810234
hg1910234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228686
Samples
Known GenesMIR4650-1, MIR4650-2, TYW1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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