A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007532



Internal ID19096751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104778962..104851593hg38UCSC Ensembl
Innerchr1:105321584..105394215hg19UCSC Ensembl
Innerchr1:105123107..105195738hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3872632
hg1972632
hg1872632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3701137
Samples
Known GenesMIR548H3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007532
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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