A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014895



Internal ID19104112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77036326..77187381hg38UCSC Ensembl
Innerchr2:77263452..77414507hg19UCSC Ensembl
Innerchr2:77116960..77268015hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38151056
hg19151056
hg18151056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582057
Samples
Known GenesLRRTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014895
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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