A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585564



Internal ID18883845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:205104414..205213516hg38UCSC Ensembl
Innerchr2:205969138..206078240hg19UCSC Ensembl
Innerchr2:205677383..205786485hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38109103
hg19109103
hg18109103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009424
Supporting Variants
Samples
Known GenesPARD3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585564
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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