A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046794



Internal ID18789325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46329015hg38UCSC Ensembl
Innerchr10:47541177..47700251hg19UCSC Ensembl
Innerchr10:47011183..47170257hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38159075
hg19159075
hg18159075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv834n100
Supporting Variantsnssv3509253
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)nsv1046794
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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