A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6604n223



Internal ID22809572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17503136..17637003hg38UCSC Ensembl
chr7:17542760..17676627hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38133868
hg19133868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6615300, nsv6617447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6604n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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