A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016239



Internal ID19105458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150086471..150103035hg38UCSC Ensembl
Innerchr6:150407607..150424171hg19UCSC Ensembl
Innerchr6:150449300..150465864hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3816565
hg1916565
hg1816565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6161n100
Supporting Variantsnssv3654465
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)nsv1016239
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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