A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025443



Internal ID18767975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10467200..10530759hg38UCSC Ensembl
Innerchr6:10467433..10530992hg19UCSC Ensembl
Innerchr6:10575419..10638978hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3863560
hg1963560
hg1863560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5917n100
Supporting Variantsnssv3654774, nssv3654773
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)nsv1025443
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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