A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6379484



Internal ID9356887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1231780..1247386hg38UCSC Ensembl
Outerchr7:1231409..1247756hg38UCSC Ensembl
Innerchr7:1271416..1287022hg19UCSC Ensembl
Outerchr7:1271045..1287392hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3816348
hg1916348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673144
Supporting Variants
SamplesHG00243
Known GenesUNCX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6379484
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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