A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004466



Internal ID70614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141930676..141931276hg38UCSC Ensembl
chr7:141630476..141631076hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477662
Supporting Variants
Samples
Known GenesCLEC5A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004466
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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