A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257385



Internal ID21400762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13104310..13122300hg38UCSC Ensembl
chr1:13171778..13189773hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3817991
hg1917996
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730073
Supporting Variants
SamplesNA19240
Known GenesHNRNPCP5
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257385
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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