A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147280



Internal ID346462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37395262..37396104hg38UCSC Ensembl
chr4:37396884..37397726hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947387
Samples
Known GenesKIAA1239
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147280
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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