A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640176



Internal ID7026951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19587374..19603877hg38UCSC Ensembl
Innerchr17:19587874..19603377hg38UCSC Ensembl
Outerchr17:19586374..19604877hg38UCSC Ensembl
chr17:19490687..19507190hg19UCSC Ensembl
Innerchr17:19491187..19506690hg19UCSC Ensembl
Outerchr17:19489687..19508190hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3816504
hg1916504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15647916, essv15647915, essv15647912, essv15647918, essv15647913, essv15647917, essv15647914
SamplesNA18917, NA19917, NA19137, HG03476, HG03024, HG02772, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640176
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer