A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173773



Internal ID15526649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15686162..15753676hg38UCSC Ensembl
Innerchr1:16012657..16080171hg19UCSC Ensembl
Innerchr1:15885244..15952758hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3867515
hg1967515
hg1867515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545614
Supporting Variants
SamplesHGDP00163
Known GenesPLEKHM2, SLC25A34, TMEM82
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173773
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