A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056586



Internal ID19145805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13197951..13775809hg38UCSC Ensembl
Innerchr21:14570272..15148130hg19UCSC Ensembl
Innerchr21:13492143..14070001hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38577859
hg19577859
hg18577859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4381n100
Supporting Variantsnssv3585280, nssv3585279, nssv3732568, nssv3585281, nssv3585282, nssv3732567
Samples
Known GenesLOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056586
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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