A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3709061



Internal ID19007342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46961233..47542082hg19UCSC Ensembl
Innerchr10:46381239..47012088hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19580850
hg18630850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035678
Supporting Variants
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35DP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3709061
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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