A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152600



Internal ID15879259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:30983506..32333459hg38UCSC Ensembl
Innerchr4:30985128..32335081hg19UCSC Ensembl
Innerchr4:30594226..31978979hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381349954
hg191349954
hg181384754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593899
Supporting Variants
SamplesHGDP01336
Known GenesPCDH7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152600
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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