A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606600



Internal ID20979671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32682001..32766500hg38UCSC Ensembl
chr7:32721613..32806112hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3884500
hg1984500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230128
Samples
Known GenesDPY19L1P1, LINC00997, MIR550A2, MIR550B2, ZNRF2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606600
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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