A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152095



Internal ID20719135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106093544..106093882hg38UCSC Ensembl
chr7:105733990..105734328hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614930
Supporting Variants
Samples
Known GenesSYPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.38235


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