A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035930



Internal ID19125149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78296629..78348824hg38UCSC Ensembl
Innerchr11:78007675..78059870hg19UCSC Ensembl
Innerchr11:77685323..77737518hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3852196
hg1952196
hg1852196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710665
Samples
Known GenesGAB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035930
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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