A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025827



Internal ID19115044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5682419..5711847hg38UCSC Ensembl
Innerchr5:5682532..5711960hg19UCSC Ensembl
Innerchr5:5735532..5764960hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3829429
hg1929429
hg1829429
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5555n100
Supporting Variantsnssv3638548, nssv3638549, nssv3638545, nssv3746164, nssv3638547, nssv3638544, nssv3638546, nssv3746165
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)nsv1025827
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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