A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034543



Internal ID19123765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..327519hg38UCSC Ensembl
Innerchr6:257341..327519hg19UCSC Ensembl
Innerchr6:202341..272519hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3870179
hg1970179
hg1870179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5877n100
Supporting Variantsnssv3651586
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)nsv1034543
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer