A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005265



Internal ID19094482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16909701..16935740hg38UCSC Ensembl
Innerchr1:17236196..17262235hg19UCSC Ensembl
Innerchr1:17108783..17134822hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3826040
hg1926040
hg1826040
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv124n100
Supporting Variantsnssv3474813, nssv3700275, nssv3471833, nssv3480980, nssv3468299, nssv3481807, nssv3464342, nssv3478638, nssv3470551, nssv3476610, nssv3478833
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005265
Frequency
Sample Size11257
Observed Gain3
Observed Loss8
Observed Complex0
Frequencyn/a


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