A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3620544



Internal ID11794638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160653405..160653504hg38UCSC Ensembl
chr5:160080412..160080511hg19UCSC Ensembl
chr5:160012990..160013089hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38100
hg19100
hg18100
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1140729
Supporting Variants
SamplesHuRef
Known GenesATP10B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3620544
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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