A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035768



Internal ID19124987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16508893..16557019hg38UCSC Ensembl
Innerchr11:16530440..16578566hg19UCSC Ensembl
Innerchr11:16487016..16535142hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3848127
hg1948127
hg1848127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708520, nssv3519060
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035768
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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