A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611889



Internal ID20984960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15256391..15318049hg38UCSC Ensembl
chr7:15296016..15357674hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3861659
hg1961659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156368
Samples
Known GenesAGMO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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