A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025776



Internal ID19114993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103270719..103314174hg38UCSC Ensembl
Innerchr6:103718594..103762049hg19UCSC Ensembl
Innerchr6:103825287..103868742hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3843456
hg1943456
hg1843456
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6118n100
Supporting Variantsnssv3649889, nssv3649891, nssv3649890, nssv3649888, nssv3649887
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)nsv1025776
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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