A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852986



Internal ID22627921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139667828..139669347hg38UCSC Ensembl
chr7:139352574..139354093hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381520
hg191520
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502064
Samples
Known GenesHIPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852986
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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