A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15720741



Internal ID1688359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63397702..63398559hg38UCSC Ensembl
Innerchr17:63397752..63398509hg38UCSC Ensembl
Outerchr17:63397626..63398635hg38UCSC Ensembl
chr17:61475063..61475920hg19UCSC Ensembl
Innerchr17:61475113..61475870hg19UCSC Ensembl
Outerchr17:61474987..61475996hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640991
Supporting Variants
SamplesHG01565
Known GenesTANC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15720741
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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