A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601888



Internal ID20974959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38359339..38362108hg38UCSC Ensembl
chr7:38398940..38401709hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382770
hg192770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156516
Samples
Known GenesTRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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