A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009924



Internal ID19099143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:208940937..209177848hg38UCSC Ensembl
Innerchr2:209805661..210042572hg19UCSC Ensembl
Innerchr2:209513906..209750817hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38236912
hg19236912
hg18236912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3585606
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)nsv1009924
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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