A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906880



Internal ID15854150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38728835..38743837hg38UCSC Ensembl
Innerchr2:38955977..38970979hg19UCSC Ensembl
Innerchr2:38809481..38824483hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3815003
hg1915003
hg1815003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581489
Supporting Variants
Samples
Known GenesGALM, SRSF7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv906880
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