A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602967



Internal ID6990000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163761578..163823918hg38UCSC Ensembl
Innerchr4:163761606..163823891hg38UCSC Ensembl
Outerchr4:163761551..163823946hg38UCSC Ensembl
chr4:164682730..164745070hg19UCSC Ensembl
Innerchr4:164682758..164745043hg19UCSC Ensembl
Outerchr4:164682703..164745098hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3862341
hg1962341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11675006
SamplesNA11930
Known GenesMARCH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602967
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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