A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11735932



Internal ID1642155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185293592..185301377hg38UCSC Ensembl
Innerchr4:185293621..185301349hg38UCSC Ensembl
Outerchr4:185293564..185301406hg38UCSC Ensembl
chr4:186214746..186222531hg19UCSC Ensembl
Innerchr4:186214775..186222503hg19UCSC Ensembl
Outerchr4:186214718..186222560hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg387786
hg197786
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603490
Supporting Variants
SamplesHG01512
Known GenesSNX25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11735932
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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