A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640380



Internal ID6680467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32352116..32357509hg38UCSC Ensembl
Innerchr17:32352161..32357464hg38UCSC Ensembl
Outerchr17:32352071..32357554hg38UCSC Ensembl
chr17:30679135..30684528hg19UCSC Ensembl
Innerchr17:30679180..30684483hg19UCSC Ensembl
Outerchr17:30679090..30684573hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg385394
hg195394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15659292, essv15659293
SamplesHG03730, HG03854
Known GenesZNF207
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640380
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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