A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157044



Internal ID20724084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27743796..27744104hg38UCSC Ensembl
chr7:27783415..27783723hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617363
Supporting Variants
Samples
Known GenesTAX1BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157044
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.86068


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