A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001314



Internal ID18743845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108930151..108955511hg38UCSC Ensembl
Innerchr1:109472773..109498133hg19UCSC Ensembl
Innerchr1:109274296..109299656hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3825361
hg1925361
hg1825361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv251n100
Supporting Variantsnssv3484528
Samples
Known GenesCLCC1, GPSM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001314
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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