A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025862



Internal ID18768394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27512448..27637542hg38UCSC Ensembl
Innerchr6:27480227..27605321hg19UCSC Ensembl
Innerchr6:27588206..27713300hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38125095
hg19125095
hg18125095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5937n100
Supporting Variantsnssv3655758
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)nsv1025862
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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