A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519572



Internal ID18817853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46247355..47743504hg19UCSC Ensembl
Innerchr10:45567361..47213510hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg191496150
hg181646150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051387
Supporting Variants
Samples
Known GenesAGAP4, AGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P1, BMS1P2, BMS1P5, BMS1P6, FAM21C, FAM25B, FAM25C, FAM25G, FAM35BP, FAM35DP, FRMPD2P1, GLUD1P7, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, PTPN20A, PTPN20B, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519572
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer