A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029980



Internal ID19119199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:356103..378703hg38UCSC Ensembl
Innerchr6:356103..378703hg19UCSC Ensembl
Innerchr6:301103..323703hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3822601
hg1922601
hg1822601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5907n100
Supporting Variantsnssv3654689
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)nsv1029980
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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