A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040042



Internal ID19129261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47090539..47742076hg19UCSC Ensembl
Innerchr10:46510545..47212082hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19651538
hg18701538
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv787n100
Supporting Variantsnssv3518624, nssv3513309
Samples
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25B, FAM25C, FAM25G, FAM35DP, HNRNPA1P33, LINC00842
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040042
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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