A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155999



Internal ID20723039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30924900..30929197hg38UCSC Ensembl
chr7:30964515..30968812hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg384298
hg194298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605076
Supporting Variants
Samples
Known GenesAQP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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