A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13039846



Internal ID3041662
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615676
Supporting Variants
SamplesHG03394
Known GenesLMBR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13039846
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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