A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020330



Internal ID19109549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69469701..69513415hg38UCSC Ensembl
Innerchr6:70179593..70223307hg19UCSC Ensembl
Innerchr6:70236314..70280028hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3843715
hg1943715
hg1843715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6014n100
Supporting Variantsnssv3658801
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)nsv1020330
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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