A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485851



Internal ID263232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104990213..104990284hg38UCSC Ensembl
chr7:104630660..104630731hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003064
Samples
Known GenesLINC01004
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485851
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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