A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749581



Internal ID18701176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161948825..162054024hg38UCSC Ensembl
Innerchr6:162369857..162475056hg19UCSC Ensembl
Innerchr6:162289847..162395046hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38105200
hg19105200
hg18105200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028447
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)nssv3749581
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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