A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706047



Internal ID18657642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46372244hg38UCSC Ensembl
Innerchr10:47541177..47743504hg19UCSC Ensembl
Innerchr10:47011183..47213510hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38202304
hg19202328
hg18202328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038081
Supporting Variants
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)nssv3706047
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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