A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035554



Internal ID19124773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62210120..62237473hg38UCSC Ensembl
Innerchr11:61977592..62004945hg19UCSC Ensembl
Innerchr11:61734168..61761521hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3827354
hg1927354
hg1827354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503901
Samples
Known GenesSCGB2A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035554
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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