A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028281



Internal ID19117499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170493636..170532993hg38UCSC Ensembl
Innerchr6:170802724..170842081hg19UCSC Ensembl
Innerchr6:170644649..170684006hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3839358
hg1939358
hg1839358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6207n100
Supporting Variantsnssv3653095, nssv3749719, nssv3653096, nssv3749720
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)nsv1028281
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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