A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998994



Internal ID66900
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 StatusS
Merged Variantsnsv5555138
Supporting Variants
Samples
Known GenesKIAA1324L
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998994
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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