A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729332



Internal ID19027613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:204624930..205211289hg38UCSC Ensembl
Innerchr2:205489653..206076013hg19UCSC Ensembl
Innerchr2:205197898..205784258hg18UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38586360
hg19586361
hg18586361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010210
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)nssv3729332
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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