A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4236774



Internal ID11172626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39894075..39894075hg38UCSC Ensembl
chr15:40186276..40186276hg19UCSC Ensembl
chr15:37973568..37973568hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3898
hg1998
hg1898
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1572077
Supporting Variants
SamplesHuRef
Known GenesGPR176
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4236774
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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