A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012872



Internal ID19102089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43960004..43981217hg38UCSC Ensembl
Innerchr2:44187143..44208356hg19UCSC Ensembl
Innerchr2:44040647..44061860hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3821214
hg1921214
hg1821214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581584
Samples
Known GenesLRPPRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012872
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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