A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003555



Internal ID18746086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:70949452..71006192hg38UCSC Ensembl
Innerchr1:71415135..71471875hg19UCSC Ensembl
Innerchr1:71187723..71244463hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3856741
hg1956741
hg1856741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv177n100
Supporting Variantsnssv3466339
Samples
Known GenesPTGER3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003555
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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