A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602724



Internal ID20975795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111129078..111160171hg38UCSC Ensembl
chr7:110769134..110800227hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3831094
hg1931094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225080
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602724
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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