A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3700662



Internal ID18998943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49387474..49464868hg38UCSC Ensembl
Innerchr1:49853146..49930540hg19UCSC Ensembl
Innerchr1:49625733..49703127hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3877395
hg1977395
hg1877395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006879
Supporting Variants
Samples
Known GenesAGBL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3700662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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