A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257702



Internal ID21400195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54222128..54321385hg38UCSC Ensembl
chr7:54289821..54389078hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3899258
hg1999258
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730048
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257702
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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