A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4170702



Internal ID11106554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151899071..151899520hg38UCSC Ensembl
chr6:152220206..152220655hg19UCSC Ensembl
chr6:152261899..152262348hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38450
hg19450
hg18450
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1599352
Supporting Variants
SamplesHuRef
Known GenesESR1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4170702
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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