A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1140845



Internal ID11957282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51652566..51652892hg38UCSC Ensembl
chr6:51517364..51517690hg19UCSC Ensembl
chr6:51625323..51625649hg18UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38327
hg19327
hg18327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3917557
SamplesHuRef
Known GenesPKHD1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1140845
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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