A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017729



Internal ID19106946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91890979..92497061hg38UCSC Ensembl
Innerchr6:92600697..93206779hg19UCSC Ensembl
Innerchr6:92657418..93263500hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38606083
hg19606083
hg18606083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3751235
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)nsv1017729
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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