A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604291



Internal ID20977362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46436068..46436776hg38UCSC Ensembl
chr7:46475666..46476374hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155356
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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