A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025236



Internal ID18767768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162229945..162466513hg38UCSC Ensembl
Innerchr6:162650977..162887545hg19UCSC Ensembl
Innerchr6:162570967..162807535hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38236569
hg19236569
hg18236569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6177n100
Supporting Variantsnssv3749590
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)nsv1025236
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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