A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048900



Internal ID19138119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47068215..47392320hg19UCSC Ensembl
Innerchr10:46488221..46812326hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19324106
hg18324106
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv792n100
Supporting Variantsnssv3503555, nssv3515528, nssv3512837, nssv3705914, nssv3506594, nssv3517181, nssv3705915, nssv3705917, nssv3508821, nssv3705918, nssv3506464, nssv3705919, nssv3507791, nssv3505601, nssv3507875, nssv3522593, nssv3504394, nssv3705916
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, 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)nsv1048900
Frequency
Sample Size11257
Observed Gain15
Observed Loss3
Observed Complex0
Frequencyn/a


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