A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017412



Internal ID18759946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161644335..161926024hg38UCSC Ensembl
Innerchr6:162065367..162347056hg19UCSC Ensembl
Innerchr6:161985357..162267046hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38281690
hg19281690
hg18281690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6169n100
Supporting Variantsnssv3749578
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)nsv1017412
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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