A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600512



Internal ID20973583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44636018..44644171hg38UCSC Ensembl
chr7:44675617..44683770hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg388154
hg198154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154610
Samples
Known GenesOGDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600512
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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