A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014197



Internal ID19103417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52992065..53063500hg38UCSC Ensembl
Innerchr2:53219203..53290638hg19UCSC Ensembl
Innerchr2:53072707..53144142hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3871436
hg1971436
hg1871436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3841n100
Supporting Variantsnssv3576617
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)nsv1014197
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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