A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4259617



Internal ID11542155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:233562718..233577851hg38UCSC Ensembl
chr2:234471364..234486497hg19UCSC Ensembl
chr2:234136102..234151235hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3815134
hg1915134
hg1815134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1030429
Supporting Variants
SamplesHuRef
Known GenesUSP40
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4259617
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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