A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019778



Internal ID18762313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162300763..162469170hg38UCSC Ensembl
Innerchr6:162721795..162890202hg19UCSC Ensembl
Innerchr6:162641785..162810192hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38168408
hg19168408
hg18168408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6185n100
Supporting Variantsnssv3654588
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)nsv1019778
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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