A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145197



Internal ID344402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45070874..45076500hg38UCSC Ensembl
chr15:45363072..45368698hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg385627
hg195627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701650
Samples
Known GenesSORD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145197
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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