A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4185626



Internal ID11121478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237544825..237545167hg38UCSC Ensembl
chr2:238453468..238453810hg19UCSC Ensembl
chr2:238118207..238118549hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38343
hg19343
hg18343
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1581868
Supporting Variants
SamplesHuRef
Known GenesMLPH
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4185626
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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