A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14090152



Internal ID4091968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35156506..35162212hg38UCSC Ensembl
Innerchr11:35156514..35162204hg38UCSC Ensembl
Outerchr11:35156498..35162220hg38UCSC Ensembl
chr11:35178053..35183759hg19UCSC Ensembl
Innerchr11:35178061..35183751hg19UCSC Ensembl
Outerchr11:35178045..35183767hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385707
hg195707
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625923
Supporting Variants
SamplesNA19207
Known GenesCD44
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14090152
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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