A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479783



Internal ID257300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156419406..156419503hg38UCSC Ensembl
chr7:156212100..156212197hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479783
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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