A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053200



Internal ID18795731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46195678..46372244hg38UCSC Ensembl
Innerchr10:47566914..47743504hg19UCSC Ensembl
Innerchr10:47036920..47213510hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38176567
hg19176591
hg18176591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv837n100
Supporting Variantsnssv3521629
Samples
Known GenesANTXRL, ANTXRLP1, FAM25B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053200
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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