A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16477354



Internal ID19340914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8086388..8086388hg38UCSC Ensembl
chr12:8238984..8238984hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3653501
Supporting Variants
Samples
Known GenesNECAP1
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)essv16477354
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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