A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653294



Internal ID15389946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46990728..47611631hg19UCSC Ensembl
Innerchr10:46410734..47081637hg18UCSC Ensembl
Innerchr10:46410734..47081637hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19620904
hg18670904
hg17670904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516485
Supporting Variants
Samples
Known GenesAGAP9, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35DP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653294
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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