A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007615



Internal ID18750146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269444..25334998hg38UCSC Ensembl
Innerchr1:25595935..25661489hg19UCSC Ensembl
Innerchr1:25468522..25534076hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3865555
hg1965555
hg1865555
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv137n100
Supporting Variantsnssv3470240, nssv3476683, nssv3466647, nssv3698493, nssv3466531, nssv3698494, nssv3474706
Samples
Known GenesRHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007615
Frequency
Sample Size29084
Observed Gain2
Observed Loss5
Observed Complex0
Frequencyn/a


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