A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603029



Internal ID20976100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27916434..27988035hg38UCSC Ensembl
chr7:27956053..28027654hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg3871602
hg1971602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157056
Samples
Known GenesJAZF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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