A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051399



Internal ID18793930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46332711..46486346hg38UCSC Ensembl
Innerchr10:47063106..47249575hg19UCSC Ensembl
Innerchr10:46483112..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38153636
hg19186470
hg18186470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv817n100
Supporting Variantsnssv3519577
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051399
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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