A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005935



Internal ID19095153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:805477..915295hg38UCSC Ensembl
Innerchr1:740857..850675hg19UCSC Ensembl
Innerchr1:730720..840538hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38109819
hg19109819
hg18109819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696752
Samples
Known GenesFAM41C, FAM87B, LINC00115, LINC01128
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005935
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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