A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043950



Internal ID19133169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46961233..47392320hg19UCSC Ensembl
Innerchr10:46381239..46812326hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19431088
hg18431088
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv755n100
Supporting Variantsnssv3504600, nssv3514072, nssv3508455, nssv3520586, nssv3709060, nssv3709059, nssv3505274, nssv3514905, nssv3521133
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)nsv1043950
Frequency
Sample Size11257
Observed Gain5
Observed Loss4
Observed Complex0
Frequencyn/a


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