A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001191



Internal ID18743722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:179128111..179151803hg38UCSC Ensembl
Innerchr1:179097246..179120938hg19UCSC Ensembl
Innerchr1:177363869..177387561hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3823693
hg1923693
hg1823693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3484380
Samples
Known GenesABL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001191
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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