A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025880



Internal ID19115097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:46000661..46389159hg38UCSC Ensembl
Innerchr5:46000763..46389261hg19UCSC Ensembl
Innerchr5:46036520..46425018hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38388499
hg19388499
hg18388499
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3637899, nssv3637898, nssv3637901, nssv3637900
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)nsv1025880
Frequency
Sample Size11257
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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