A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488578



Internal ID265883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32501281..32502090hg38UCSC Ensembl
chr10:32790209..32791018hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032004
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488578
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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