A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386997



Internal ID21044550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75769701..75770700hg38UCSC Ensembl
chr4:76690854..76691853hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120226
Samples
Known GenesUSO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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