A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604585



Internal ID20977656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15542391..15582722hg38UCSC Ensembl
chr7:15582016..15622347hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3840332
hg1940332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151400
Samples
Known GenesAGMO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604585
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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