A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048876



Internal ID18791407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46175087..46317039hg38UCSC Ensembl
Innerchr10:47546323..47688275hg19UCSC Ensembl
Innerchr10:47016329..47158281hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38141953
hg19141953
hg18141953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n100
Supporting Variantsnssv3706066
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)nsv1048876
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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