A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014587



Internal ID18757122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:110097959..110226092hg38UCSC Ensembl
Innerchr2:110855536..110983669hg19UCSC Ensembl
Innerchr2:110212825..110340958hg18UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38128134
hg19128134
hg18128134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4046n100
Supporting Variantsnssv3580202, nssv3580203
Samples
Known GenesLINC00116, MALL, NPHP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014587
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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