A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044887



Internal ID19134106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64683335..64740951hg38UCSC Ensembl
Innerchr13:65257467..65315083hg19UCSC Ensembl
Innerchr13:64155468..64213084hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3857617
hg1957617
hg1857617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1698n100
Supporting Variantsnssv3526801
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)nsv1044887
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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