A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749597



Internal ID18701192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162324536..162380313hg38UCSC Ensembl
Innerchr6:162745568..162801345hg19UCSC Ensembl
Innerchr6:162665558..162721335hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3855778
hg1955778
hg1855778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033809
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)nssv3749597
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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