A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844386



Internal ID22619321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136414519..136418918hg38UCSC Ensembl
chr6:136735657..136740056hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501750
Samples
Known GenesMAP7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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