A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159531



Internal ID20726571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74381364..74386135hg38UCSC Ensembl
chr7:73795694..73800465hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384772
hg194772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611187
Supporting Variants
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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