A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383717



Internal ID21041270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173317901..173319500hg38UCSC Ensembl
chr4:174239052..174240651hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112354
Samples
Known GenesGALNT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383717
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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