A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600568



Internal ID20973639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11591545..11592104hg38UCSC Ensembl
chr7:11631172..11631731hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153571
Samples
Known GenesTHSD7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600568
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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