A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15629339



Internal ID4121206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16010559..16016585hg38UCSC Ensembl
Innerchr17:16010559..16016585hg38UCSC Ensembl
Outerchr17:16010342..16016833hg38UCSC Ensembl
chr17:15913873..15919899hg19UCSC Ensembl
Innerchr17:15913873..15919899hg19UCSC Ensembl
Outerchr17:15913656..15920147hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg386027
hg196027
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640094
Supporting Variants
SamplesHG03740
Known GenesTTC19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15629339
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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