A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3765321



Internal ID11649864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71680109..71680397hg38UCSC Ensembl
chr7:71145094..71145382hg19UCSC Ensembl
chr7:70783030..70783318hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1489524
Supporting Variants
SamplesHuRef
Known GenesWBSCR17
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3765321
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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