A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012560



Internal ID19101777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89365010..89958690hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg18593681
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3968n100
Supporting Variantsnssv3582595, nssv3582586, nssv3582585, nssv3582578, nssv3582575, nssv3582593, nssv3730043, nssv3730045, nssv3582588, nssv3582572, nssv3730044, nssv3582582, nssv3582576, nssv3582574, nssv3582583, nssv3582580, nssv3582577, nssv3582594, nssv3582584, nssv3730046, nssv3582589, nssv3582581, nssv3582590, nssv3582592, nssv3582573, nssv3582579, nssv3582591, nssv3582587
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012560
Frequency
Sample Size11257
Observed Gain18
Observed Loss10
Observed Complex0
Frequencyn/a


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