A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580097



Internal ID18878378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:99863970..99985124hg38UCSC Ensembl
Innerchr2:100480432..100601586hg19UCSC Ensembl
Innerchr2:99846864..99968018hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38121155
hg19121155
hg18121155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003114
Supporting Variants
Samples
Known GenesAFF3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580097
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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