A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018466



Internal ID19107683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161395629..161439604hg38UCSC Ensembl
Innerchr6:161816661..161860636hg19UCSC Ensembl
Innerchr6:161736651..161780626hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3843976
hg1943976
hg1843976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6168n100
Supporting Variantsnssv3749577, nssv3654522, nssv3654521, nssv3654519, nssv3654524, nssv3654523, nssv3654525, nssv3654518, nssv3654517, nssv3749576, nssv3654520, nssv3654516
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)nsv1018466
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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