A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615419



Internal ID7002308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148897627..148922819hg38UCSC Ensembl
Innerchr7:148898127..148922319hg38UCSC Ensembl
Outerchr7:148896627..148923819hg38UCSC Ensembl
chr7:148594719..148619911hg19UCSC Ensembl
Innerchr7:148595219..148619411hg19UCSC Ensembl
Outerchr7:148593719..148620911hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3825193
hg1925193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1334e214
Supporting Variantsessv13003719
SamplesNA19011
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615419
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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