A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011778



Internal ID19100996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:139270050..139369958hg38UCSC Ensembl
Innerchr2:140027620..140127528hg19UCSC Ensembl
Innerchr2:139744090..139843998hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3899909
hg1999909
hg1899909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582802
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)nsv1011778
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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