A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021359



Internal ID19110576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:81053956..81110216hg38UCSC Ensembl
Innerchr6:81763673..81819933hg19UCSC Ensembl
Innerchr6:81820392..81876652hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3856261
hg1956261
hg1856261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648868
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)nsv1021359
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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