A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377611



Internal ID21035164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37271001..37273800hg38UCSC Ensembl
chr4:37272623..37275422hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115946
Samples
Known GenesKIAA1239
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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