A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027600



Internal ID19116819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:67851590..67932853hg38UCSC Ensembl
Innerchr6:68561483..68642745hg19UCSC Ensembl
Innerchr6:68618204..68699466hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3881264
hg1981263
hg1881263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6013n100
Supporting Variantsnssv3658795
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)nsv1027600
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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