A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149164



Internal ID20716204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111289102..111555583hg38UCSC Ensembl
chr7:110929158..111195639hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38266482
hg19266482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611151
Supporting Variants
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149164
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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