A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4297368



Internal ID11579906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108188819..108188819hg38UCSC Ensembl
chr7:107829263..107829263hg19UCSC Ensembl
chr7:107616499..107616499hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg386068
hg196068
hg186068
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1781344
Supporting Variants
SamplesHuRef
Known GenesNRCAM
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4297368
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer