A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617633



Internal ID20990704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8009435..8025453hg38UCSC Ensembl
chr7:8049065..8065083hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3816019
hg1916019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219352
Samples
Known GenesGLCCI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617633
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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