A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11360356



Internal ID6476554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16334870..16374653hg38UCSC Ensembl
Innerchr4:16334880..16374644hg38UCSC Ensembl
Outerchr4:16334861..16374663hg38UCSC Ensembl
chr4:16336493..16376276hg19UCSC Ensembl
Innerchr4:16336503..16376267hg19UCSC Ensembl
Outerchr4:16336484..16376286hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3839784
hg1939784
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599753
Supporting Variants
SamplesNA20522
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11360356
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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