A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615233



Internal ID6655432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140472880..140474333hg38UCSC Ensembl
Innerchr7:140472919..140474295hg38UCSC Ensembl
Outerchr7:140472842..140474372hg38UCSC Ensembl
chr7:140172680..140174133hg19UCSC Ensembl
Innerchr7:140172719..140174095hg19UCSC Ensembl
Outerchr7:140172642..140174172hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381454
hg191454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12983110
SamplesNA11881
Known GenesMKRN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615233
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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