A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3777296



Internal ID11637889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30632178..30632178hg38UCSC Ensembl
chr15:30924381..30924381hg19UCSC Ensembl
chr15:28711673..28711673hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38593
hg19593
hg18593
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1523587
Supporting Variants
SamplesHuRef
Known GenesARHGAP11B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3777296
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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