A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600131



Internal ID18551726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33647795..33688348hg38UCSC Ensembl
Innerchr21:35020101..35060653hg19UCSC Ensembl
Innerchr21:33941971..33982523hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3840554
hg1940553
hg1840553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059744
Supporting Variants
Samples
Known GenesITSN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600131
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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