A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157029



Internal ID20724069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27538514..27539208hg38UCSC Ensembl
chr7:27578133..27578827hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607087
Supporting Variants
Samples
Known GenesHIBADH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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