A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3674577



Internal ID19392585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160407644..160407877hg38UCSC Ensembl
chr2:161264155..161264388hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16496322
Samples
Known GenesMIR4785, RBMS1
MethodSequencing
Analysisde novo assemblies produced from SoapDenovo2 were aligned to GRC37 using LAST and input into SoapAsmVar for population-wide structural variation detection. The method is described in the publication
PlatformIllumina HiSeq 2000
Comments
ReferenceBesenbacher_et_al_2015
Pubmed ID25597990
Accession Number(s)esv3674577
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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