A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025253



Internal ID19114471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..71201hg38UCSC Ensembl
Innerchr5:15520..71316hg19UCSC Ensembl
Innerchr5:68520..124316hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3855682
hg1955797
hg1855797
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5512n100
Supporting Variantsnssv3636508, nssv3636507, nssv3636509, nssv3636504, nssv3636505, nssv3636510, nssv3636506
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)nsv1025253
Frequency
Sample Size11257
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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