A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023163



Internal ID18765696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10468433..10530759hg38UCSC Ensembl
Innerchr6:10468666..10530992hg19UCSC Ensembl
Innerchr6:10576652..10638978hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3862327
hg1962327
hg1862327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5917n100
Supporting Variantsnssv3654782, nssv3654775, nssv3654778, nssv3654780, nssv3654779, nssv3654776, nssv3654781, nssv3654777
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)nsv1023163
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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