A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4015780



Internal ID11746093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:820471..820783hg38UCSC Ensembl
chr17:723711..724023hg19UCSC Ensembl
chr17:670461..670773hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38313
hg19313
hg18313
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1468501
Supporting Variants
SamplesHuRef
Known GenesNXN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4015780
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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