A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4017753



Internal ID11744120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:835708..836108hg38UCSC Ensembl
chr17:738948..739348hg19UCSC Ensembl
chr17:685698..686098hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38401
hg19401
hg18401
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1262780
Supporting Variants
SamplesHuRef
Known GenesNXN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4017753
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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