A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13907919



Internal ID3909735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97274984..97277481hg38UCSC Ensembl
Innerchr10:97275111..97277431hg38UCSC Ensembl
Outerchr10:97274764..97277701hg38UCSC Ensembl
chr10:99034741..99037238hg19UCSC Ensembl
Innerchr10:99034868..99037188hg19UCSC Ensembl
Outerchr10:99034521..99037458hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382498
hg192498
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624311
Supporting Variants
SamplesNA19984
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13907919
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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