A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023598



Internal ID19112815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40747919..40856677hg38UCSC Ensembl
Innerchr6:40715658..40824416hg19UCSC Ensembl
Innerchr6:40823636..40932394hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38108759
hg19108759
hg18108759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657431
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)nsv1023598
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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