A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610279



Internal ID20983350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39718782..39751749hg38UCSC Ensembl
chr7:39758381..39791348hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3832968
hg1932968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227350
Samples
Known GenesLINC00265
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610279
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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