A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4033555



Internal ID11381633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88501107..88501462hg38UCSC Ensembl
chr16:88567515..88567870hg19UCSC Ensembl
chr16:87095016..87095371hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38356
hg19356
hg18356
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1139853
Supporting Variants
SamplesHuRef
Known GenesZFPM1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4033555
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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