A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027141



Internal ID19116360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153656535..153712427hg38UCSC Ensembl
Innerchr6:153977670..154033562hg19UCSC Ensembl
Innerchr6:154019363..154075255hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3855893
hg1955893
hg1855893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6164n100
Supporting Variantsnssv3654478, nssv3749564
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)nsv1027141
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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