A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1399069



Internal ID12215505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:675530..675905hg38UCSC Ensembl
chr6:675530..675905hg19UCSC Ensembl
chr6:620530..620905hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38376
hg19376
hg18376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3891436
SamplesHuRef
Known GenesEXOC2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1399069
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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