A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417730



Internal ID21075283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135876425..135883525hg38UCSC Ensembl
chr7:135561173..135568273hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg387101
hg197101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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