A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655379



Internal ID18606974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162537326..162618673hg38UCSC Ensembl
Innerchr6:162958358..163039705hg19UCSC Ensembl
Innerchr6:162878348..162959695hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3881348
hg1981348
hg1881348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034971
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)nssv3655379
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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