A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617867



Internal ID20990938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102327148..102380454hg38UCSC Ensembl
chr7:101967566..102020901hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3853307
hg1953336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226128
Samples
Known GenesLOC100289561, LOC100630923, SPDYE6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617867
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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