A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053512



Internal ID19142731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130859989..130870528hg38UCSC Ensembl
Innerchr9:133735376..133745915hg19UCSC Ensembl
Innerchr9:132725197..132735736hg18UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3810540
hg1910540
hg1810540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695285
Samples
Known GenesABL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053512
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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