A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641737



Internal ID7028508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9205196..9206976hg38UCSC Ensembl
Innerchr18:9205196..9206976hg38UCSC Ensembl
Outerchr18:9204991..9207186hg38UCSC Ensembl
chr18:9205194..9206974hg19UCSC Ensembl
Innerchr18:9205194..9206974hg19UCSC Ensembl
Outerchr18:9204989..9207184hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381781
hg191781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15797894, essv15797892, essv15797891, essv15797893
SamplesNA12414, NA20525, HG02445, HG00256
Known GenesANKRD12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641737
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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