A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014577



Internal ID19103795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35447316..35489858hg38UCSC Ensembl
Innerchr2:35672382..35714924hg19UCSC Ensembl
Innerchr2:35525886..35568428hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3842543
hg1942543
hg1842543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581240
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)nsv1014577
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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