A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3696101



Internal ID12065769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:893850..893994hg38UCSC Ensembl
chr17:797090..797234hg19UCSC Ensembl
chr17:743840..743984hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38145
hg19145
hg18145
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1098416
Supporting Variants
SamplesHuRef
Known GenesNXN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3696101
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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