A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832729



Internal ID22607664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214512655..214514519hg38UCSC Ensembl
chr2:215377379..215379243hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381865
hg191865
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482633
Samples
Known GenesVWC2L, VWC2L-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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