A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600192



Internal ID18551787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37045398..37132761hg38UCSC Ensembl
Innerchr21:38417698..38505061hg19UCSC Ensembl
Innerchr21:37339568..37426931hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3887364
hg1987364
hg1887364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066107
Supporting Variants
Samples
Known GenesPIGP, TTC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600192
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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