A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045078



Internal ID18787609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79169373..79198440hg38UCSC Ensembl
Innerchr10:80929130..80958197hg19UCSC Ensembl
Innerchr10:80599136..80628203hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3829068
hg1929068
hg1829068
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706111
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045078
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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