A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624814



Internal ID7011664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124551036..124551981hg38UCSC Ensembl
Innerchr10:124551086..124551931hg38UCSC Ensembl
Outerchr10:124550936..124552081hg38UCSC Ensembl
chr10:126239605..126240550hg19UCSC Ensembl
Innerchr10:126239655..126240500hg19UCSC Ensembl
Outerchr10:126239505..126240650hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963288, essv13963289
SamplesNA19108, HG02855
Known GenesLHPP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624814
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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