A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026517



Internal ID19115735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76912593..77117701hg38UCSC Ensembl
Innerchr6:77622310..77827418hg19UCSC Ensembl
Innerchr6:77679029..77884137hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38205109
hg19205109
hg18205109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6022n100
Supporting Variantsnssv3659052
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)nsv1026517
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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