A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014043



Internal ID19103263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76317328..76358622hg38UCSC Ensembl
Innerchr2:76544454..76585748hg19UCSC Ensembl
Innerchr2:76397962..76439256hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3841295
hg1941295
hg1841295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3873n100
Supporting Variantsnssv3582007
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)nsv1014043
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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