A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045782



Internal ID18788313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46332711..46455455hg38UCSC Ensembl
Innerchr10:47094305..47249575hg19UCSC Ensembl
Innerchr10:46514311..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38122745
hg19155271
hg18155271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv817n100
Supporting Variantsnssv3515562
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, HNRNPA1P33, LINC00842
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045782
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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