A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028517



Internal ID18771048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10470804..10530759hg38UCSC Ensembl
Innerchr6:10471037..10530992hg19UCSC Ensembl
Innerchr6:10579023..10638978hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3859956
hg1959956
hg1859956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5917n100
Supporting Variantsnssv3654783
Samples
Known GenesGCNT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028517
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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