A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009664



Internal ID18752195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16636806..16686278hg38UCSC Ensembl
Innerchr1:16963301..17012773hg19UCSC Ensembl
Innerchr1:16835888..16885360hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3849473
hg1949473
hg1849473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv71n100
Supporting Variantsnssv3467864
Samples
Known GenesLOC729574, MIR3675, MST1P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009664
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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