A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600104



Internal ID18898385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:28081544..28126948hg38UCSC Ensembl
Innerchr21:29453863..29499267hg19UCSC Ensembl
Innerchr21:28375734..28421138hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3845405
hg1945405
hg1845405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061909
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600104
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