A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656961



Internal ID15393613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46990728..47640344hg19UCSC Ensembl
Innerchr10:46410734..47110350hg18UCSC Ensembl
Innerchr10:46410734..47110350hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19649617
hg18699617
hg17699617
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)nssv656961
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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