A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485434



Internal ID262823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156531943..156542821hg38UCSC Ensembl
chr7:156324637..156335515hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3810879
hg1910879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006912
Samples
Known GenesLINC00244, LINC01006
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485434
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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