A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550725



Internal ID16338134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47028331..47741882hg19UCSC Ensembl
Innerchr10:46448337..47211888hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19713552
hg18763552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747368
Samples
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25B, FAM25C, FAM25G, FAM35DP, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550725
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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