A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147691



Internal ID20714731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100253627..100255333hg38UCSC Ensembl
chr7:99851250..99852956hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381707
hg191707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610620
Supporting Variants
Samples
Known GenesGATS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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