A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153089



Internal ID20720129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34872401..34874200hg38UCSC Ensembl
chr7:34912013..34913812hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609316
Supporting Variants
Samples
Known GenesNPSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00346


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