A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045822



Internal ID19135041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123753338..123786166hg38UCSC Ensembl
Innerchr10:125512854..125545682hg19UCSC Ensembl
Innerchr10:125502844..125535672hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3832829
hg1932829
hg1832829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv988n100
Supporting Variantsnssv3515598
Samples
Known GenesCPXM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045822
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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