A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050149



Internal ID18792680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46277639hg38UCSC Ensembl
Innerchr10:47541177..47648875hg19UCSC Ensembl
Innerchr10:47011183..47118881hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38107699
hg19107699
hg18107699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv831n100
Supporting Variantsnssv3519431
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)nsv1050149
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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