A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023664



Internal ID18766197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162116071..162143022hg38UCSC Ensembl
Innerchr6:162537103..162564054hg19UCSC Ensembl
Innerchr6:162457093..162484044hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3826952
hg1926952
hg1826952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749584
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)nsv1023664
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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