A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729788



Internal ID19028069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88844243..89201738hg38UCSC Ensembl
Innerchr2:89143756..89501226hg19UCSC Ensembl
Innerchr2:88924871..89282341hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38357496
hg19357471
hg18357471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012313
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729788
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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