A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036342



Internal ID18778873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46287904hg38UCSC Ensembl
Innerchr10:47541177..47659140hg19UCSC Ensembl
Innerchr10:47011183..47129146hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38117964
hg19117964
hg18117964
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv832n100
Supporting Variantsnssv3706012, nssv3519318, nssv3509369, nssv3706013, nssv3519516, nssv3509054, nssv3506076, nssv3512723, nssv3504837, nssv3503304, nssv3505819, nssv3519814, nssv3706014, nssv3513106
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036342
Frequency
Sample Size29084
Observed Gain2
Observed Loss12
Observed Complex0
Frequencyn/a


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