A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616716



Internal ID20989787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104768853..104840833hg38UCSC Ensembl
chr7:104409300..104481280hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg3871981
hg1971981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231769
Samples
Known GenesLHFPL3, LHFPL3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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