A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999429



Internal ID18812279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16902167..17085289hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg18183123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv78n100
Supporting Variantsnssv3480034, nssv3468461
Samples
Known GenesESPNP, LOC729574, MIR3675, MST1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999429
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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