A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555138



Internal ID328304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87052952..87149103hg38UCSC Ensembl
chr7:86682268..86778419hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3896152
hg1996152
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16998994
Samples
Known GenesKIAA1324L
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555138
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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