A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027261



Internal ID18769793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161949740..162054024hg38UCSC Ensembl
Innerchr6:162370772..162475056hg19UCSC Ensembl
Innerchr6:162290762..162395046hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38104285
hg19104285
hg18104285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6173n100
Supporting Variantsnssv3654543
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)nsv1027261
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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