A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903032



Internal ID16196988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3597839..3625275hg38UCSC Ensembl
Innerchr2:3645429..3672865hg19UCSC Ensembl
Innerchr2:3623304..3650740hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3827437
hg1927437
hg1827437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580823
Supporting Variants
Samples
Known GenesCOLEC11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv903032
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