A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387276



Internal ID21044829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168581764..168582111hg38UCSC Ensembl
chr4:169502915..169503262hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115355
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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