A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147700



Internal ID20714740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100340304..100348281hg38UCSC Ensembl
chr7:99937927..99945904hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg387978
hg197978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614380
Supporting Variants
Samples
Known GenesSTAG3L5P, STAG3L5P-PVRIG2P-PILRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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