A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053502



Internal ID18796033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46279715hg38UCSC Ensembl
Innerchr10:47541177..47650951hg19UCSC Ensembl
Innerchr10:47011183..47120957hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38109775
hg19109775
hg18109775
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv832n100
Supporting Variantsnssv3508496, nssv3519082, nssv3512641, nssv3516369, nssv3705999, nssv3506359
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053502
Frequency
Sample Size29084
Observed Gain3
Observed Loss3
Observed Complex0
Frequencyn/a


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