A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557607



Internal ID330700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85630881..85631249hg38UCSC Ensembl
chr6:86340599..86340967hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985287
Samples
Known GenesSYNCRIP
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557607
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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