A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749575



Internal ID19047856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161395629..161439137hg38UCSC Ensembl
Innerchr6:161816661..161860169hg19UCSC Ensembl
Innerchr6:161736651..161780159hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3843509
hg1943509
hg1843509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018065
Supporting Variants
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)nssv3749575
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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