A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615676



Internal ID7002565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156789840..156790842hg38UCSC Ensembl
Innerchr7:156789840..156790842hg38UCSC Ensembl
Outerchr7:156789578..156791231hg38UCSC Ensembl
chr7:156582534..156583536hg19UCSC Ensembl
Innerchr7:156582534..156583536hg19UCSC Ensembl
Outerchr7:156582272..156583925hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381003
hg191003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13039849, essv13039845, essv13039842, essv13039838, essv13039848, essv13039850, essv13039837, essv13039836, essv13039847, essv13039854, essv13039841, essv13039846, essv13039835, essv13039853, essv13039851, essv13039839, essv13039844, essv13039852, essv13039840, essv13039843
SamplesNA19028, NA19204, NA19399, HG03297, HG02922, HG03520, HG02427, HG03583, HG03394, HG02442, NA19236, HG02322, HG02010, HG03458, HG01958, HG02837, HG02558, HG03097, NA19213, HG03072
Known GenesLMBR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615676
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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