A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030229



Internal ID19119448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..382897hg38UCSC Ensembl
Innerchr6:264744..382897hg19UCSC Ensembl
Innerchr6:209744..327897hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38118154
hg19118154
hg18118154
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3653600, nssv3747794, nssv3653599, nssv3653598
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)nsv1030229
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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