A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3737637



Internal ID11677547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161263105..161263207hg38UCSC Ensembl
chr6:161684137..161684239hg19UCSC Ensembl
chr6:161604127..161604229hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38103
hg19103
hg18103
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1221310
Supporting Variants
SamplesHuRef
Known GenesAGPAT4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3737637
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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