A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634884



Internal ID7021684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72099433..72104091hg38UCSC Ensembl
Innerchr14:72099448..72104076hg38UCSC Ensembl
Outerchr14:72099418..72104106hg38UCSC Ensembl
chr14:72566150..72570808hg19UCSC Ensembl
Innerchr14:72566165..72570793hg19UCSC Ensembl
Outerchr14:72566135..72570823hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg384659
hg194659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15055396, essv15055397, essv15055394, essv15055393, essv15055395
SamplesHG03978, HG03714, HG03692, HG04003, HG03896
Known GenesRGS6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634884
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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