A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605326



Internal ID20978397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44705001..44706800hg38UCSC Ensembl
chr7:44744600..44746399hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154616
Samples
Known GenesOGDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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