A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049539



Internal ID19138758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130765128..130782970hg38UCSC Ensembl
Innerchr9:133640515..133658357hg19UCSC Ensembl
Innerchr9:132630336..132648178hg18UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3817843
hg1917843
hg1817843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695283
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)nsv1049539
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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