A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004962



Internal ID19094179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:629241..915295hg38UCSC Ensembl
Innerchr1:564621..850675hg19UCSC Ensembl
Innerchr1:554484..840538hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38286055
hg19286055
hg18286055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696751
Samples
Known GenesFAM41C, FAM87B, 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)nsv1004962
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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