A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639922



Internal ID6680012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9765539..9773391hg38UCSC Ensembl
Innerchr17:9765539..9773391hg38UCSC Ensembl
Outerchr17:9765367..9773608hg38UCSC Ensembl
chr17:9668856..9676708hg19UCSC Ensembl
Innerchr17:9668856..9676708hg19UCSC Ensembl
Outerchr17:9668684..9676925hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg387853
hg197853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15610358, essv15610359, essv15610361, essv15610360
SamplesHG02645, HG02623, HG03025, HG02947
Known GenesDHRS7C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639922
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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