A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608555



Internal ID20981626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32728801..32774500hg38UCSC Ensembl
chr7:32768413..32814112hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3845700
hg1945700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6637n223
Supporting Variantsnssv18233114
Samples
Known GenesLINC00997, MIR550A2, MIR550B2, ZNRF2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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