A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732559



Internal ID18684154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13080529..13715716hg38UCSC Ensembl
Innerchr21:14452850..15088037hg19UCSC Ensembl
Innerchr21:13374721..14009908hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38635188
hg19635188
hg18635188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067043
Supporting Variants
Samples
Known GenesANKRD30BP2, LOC100288966, MIR3156-3, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3732559
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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