A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430899



Internal ID22488769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66465406..66588341hg38UCSC Ensembl
chr7:65930393..66053328hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38122936
hg19122936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913173
Supporting Variants
Samples
Known GenesLOC493754
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430899
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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