A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3734161



Internal ID11681023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63575507..63575507hg38UCSC Ensembl
chr2:63802641..63802641hg19UCSC Ensembl
chr2:63656145..63656145hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3867
hg1967
hg1867
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1071119
Supporting Variants
SamplesHuRef
Known GenesWDPCP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3734161
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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