A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040617



Internal ID19129836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55661919..55836092hg38UCSC Ensembl
Innerchr11:55429395..55603568hg19UCSC Ensembl
Innerchr11:55185971..55360144hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38174174
hg19174174
hg18174174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1204n100
Supporting Variantsnssv3503414, nssv3520552, nssv3509797, nssv3519930, nssv3517114, nssv3511376, nssv3515846, nssv3512952, nssv3505299
Samples
Known GenesOR4C6, OR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040617
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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