A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16496187



Internal ID19359747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9160810..9161428hg38UCSC Ensembl
chrY:8998419..8999037hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3674425
Supporting Variants
Samples
Known Genes
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)essv16496187
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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