A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027524



Internal ID19116743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..365708hg38UCSC Ensembl
Innerchr6:264744..365708hg19UCSC Ensembl
Innerchr6:209744..310708hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38100965
hg19100965
hg18100965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3653562, nssv3653563
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027524
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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