A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850821



Internal ID22625756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76415478..76420289hg38UCSC Ensembl
chr7:76044795..76049606hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384812
hg194812
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509320
Samples
Known GenesZP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850821
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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