A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615309



Internal ID20988380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10877448..10966787hg38UCSC Ensembl
chr7:10917075..11006414hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3889340
hg1989340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6577n223
Supporting Variantsnssv18218172
Samples
Known GenesNDUFA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615309
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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