A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038808



Internal ID19128027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34621529..34733295hg38UCSC Ensembl
Innerchr15:34913730..35025496hg19UCSC Ensembl
Innerchr15:32701022..32812788hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38111767
hg19111767
hg18111767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2575n100
Supporting Variantsnssv3552144
Samples
Known GenesMIR5588
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038808
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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