A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466368



Internal ID19061711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:629393..863579hg38UCSC Ensembl
Innerchr1:564773..798959hg19UCSC Ensembl
Innerchr1:554636..788822hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38234187
hg19234187
hg18234187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003571
Supporting Variants
Samples
Known GenesFAM87B, LINC00115, LINC01128, LOC100133331, LOC100288069, MIR6723, OR4F16, OR4F29, OR4F3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3466368
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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