A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021432



Internal ID18763966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162219715..162272516hg38UCSC Ensembl
Innerchr6:162640747..162693548hg19UCSC Ensembl
Innerchr6:162560737..162613538hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3852802
hg1952802
hg1852802
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654566
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)nsv1021432
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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