A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640436



Internal ID6680523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34993047..34994167hg38UCSC Ensembl
Innerchr17:34993047..34994167hg38UCSC Ensembl
Outerchr17:34992951..34994271hg38UCSC Ensembl
chr17:33320066..33321186hg19UCSC Ensembl
Innerchr17:33320066..33321186hg19UCSC Ensembl
Outerchr17:33319970..33321290hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15664349, essv15664344, essv15664347, essv15664345, essv15664350, essv15664346, essv15664351, essv15664348
SamplesHG03593, HG03857, HG03907, HG03928, HG03969, HG04200, HG04219, HG04080
Known GenesLIG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640436
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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