A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000966



Internal ID18743497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51071789..51108905hg38UCSC Ensembl
Innerchr2:51298927..51336043hg19UCSC Ensembl
Innerchr2:51152431..51189547hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3837117
hg1937117
hg1837117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726023, nssv3581690
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)nsv1000966
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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