A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704284



Internal ID21226089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74369858..74370156hg38UCSC Ensembl
chr7:73784188..73784486hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817083
Supporting Variants
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704284
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.553571


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