A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061525



Internal ID19150744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13240276..13715716hg38UCSC Ensembl
Innerchr21:14612597..15088037hg19UCSC Ensembl
Innerchr21:13534468..14009908hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38475441
hg19475441
hg18475441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4381n100
Supporting Variantsnssv3585319
Samples
Known GenesLOC100288966, 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)nsv1061525
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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