A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519352



Internal ID18817633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47085303..47743504hg19UCSC Ensembl
Innerchr10:46505309..47213510hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19658202
hg18708202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050068
Supporting Variants
Samples
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25B, FAM25C, FAM25G, FAM35DP, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519352
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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