A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026704



Internal ID18769235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162218055..162308495hg38UCSC Ensembl
Innerchr6:162639087..162729527hg19UCSC Ensembl
Innerchr6:162559077..162649517hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3890441
hg1990441
hg1890441
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6179n100
Supporting Variantsnssv3654564, nssv3654562, nssv3654563, nssv3654565
Samples
Known GenesPARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026704
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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