A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608702



Internal ID20981773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111123204..111283704hg38UCSC Ensembl
chr7:110763260..110923760hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38160501
hg19160501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237036
Samples
Known GenesIMMP2L, LRRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608702
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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