A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405877



Internal ID21063430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37993801..38016700hg38UCSC Ensembl
chr6:37961577..37984476hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3822900
hg1922900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221553
Samples
Known GenesZFAND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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