A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615609



Internal ID20988680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27847508..27850031hg38UCSC Ensembl
chr7:27887127..27889650hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg382524
hg192524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157050
Samples
Known GenesJAZF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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