A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528750



Internal ID15456043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45529172..45580787hg38UCSC Ensembl
Innerchr10:46024620..46076235hg19UCSC Ensembl
Innerchr10:45344626..45396241hg18UCSC Ensembl
Innerchr10:45344626..45396241hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3851616
hg1951616
hg1851616
hg1751616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705412
Samples
Known GenesMARCH8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528750
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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