A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15659292



Internal ID5661108
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640380
Supporting Variants
SamplesHG03730
Known GenesZNF207
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15659292
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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