A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12902267



Internal ID4617297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97100233..97121364hg38UCSC Ensembl
Innerchr7:97100733..97120864hg38UCSC Ensembl
Outerchr7:97099233..97122364hg38UCSC Ensembl
chr7:96729545..96750676hg19UCSC Ensembl
Innerchr7:96730045..96750176hg19UCSC Ensembl
Outerchr7:96728545..96751676hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3821132
hg1921132
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614222
Supporting Variants
SamplesHG04153
Known GenesACN9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12902267
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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