A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615628



Internal ID20988699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102703401..102826600hg38UCSC Ensembl
chr7:102343848..102467047hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38123200
hg19123200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225264
Samples
Known GenesFAM185A, FBXL13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615628
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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