A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010367



Internal ID18752898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:68470836..68492992hg38UCSC Ensembl
Innerchr1:68936519..68958675hg19UCSC Ensembl
Innerchr1:68709107..68731263hg18UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg3822157
hg1922157
hg1822157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3470751
Samples
Known GenesDEPDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010367
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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