A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009592



Internal ID19098810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109146692..109212096hg38UCSC Ensembl
Innerchr1:109689314..109754718hg19UCSC Ensembl
Innerchr1:109490837..109556241hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3865405
hg1965405
hg1865405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3487368
Samples
Known GenesKIAA1324
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009592
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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