A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024900



Internal ID19114117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..315197hg38UCSC Ensembl
Innerchr6:264744..315197hg19UCSC Ensembl
Innerchr6:209744..260197hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3850454
hg1950454
hg1850454
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5882n100
Supporting Variantsnssv3653552, nssv3747781, nssv3653553, nssv3653551
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)nsv1024900
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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