A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618629



Internal ID20991700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106491185..106516468hg38UCSC Ensembl
chr7:106131631..106156914hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3825284
hg1925284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618629
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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