A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712047



Internal ID15659317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27523427..27631734hg38UCSC Ensembl
Innerchr1:27849938..27958245hg19UCSC Ensembl
Innerchr1:27722525..27830832hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38108308
hg19108308
hg18108308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545915
Supporting Variants
Samples
Known GenesAHDC1, FGR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712047
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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