A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374914



Internal ID21032467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10034439..10748726hg38UCSC Ensembl
chr4:10036063..10750350hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38714288
hg19714288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211314
Samples
Known GenesCLNK, MIR3138, SLC2A9, WDR1, ZNF518B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374914
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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