A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026561



Internal ID19115779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3164884..3223279hg38UCSC Ensembl
Innerchr6:3165118..3223513hg19UCSC Ensembl
Innerchr6:3110117..3168512hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3858396
hg1958396
hg1858396
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654723, nssv3747902, nssv3747900, nssv3654724, nssv3747901
Samples
Known GenesLOC100507194
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026561
Frequency
Sample Size11257
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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