A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048584



Internal ID18791115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91075976..91154665hg38UCSC Ensembl
Innerchr10:92835733..92914422hg19UCSC Ensembl
Innerchr10:92825713..92904402hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3878690
hg1978690
hg1878690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706193
Samples
Known GenesNUDT9P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048584
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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