A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016548



Internal ID19105767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60591828..61119912hg38UCSC Ensembl
Innerchr6:57559575..58140288hg19UCSC Ensembl
Innerchr6:57667534..58248247hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38528085
hg19580714
hg18580714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745507
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)nsv1016548
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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