A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479669



Internal ID257185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73608000..73614779hg38UCSC Ensembl
chr7:73022330..73029109hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386780
hg196780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000005
Samples
Known GenesMLXIPL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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