A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257946



Internal ID21400038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:110095722..110602326hg38UCSC Ensembl
chr2:110853299..111359903hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38506605
hg19506605
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730141
Supporting Variants
SamplesNA19238
Known GenesLIMS3, LIMS3L, LIMS3-LOC440895, LINC00116, LINC01106, LINC01123, LOC100288570, LOC100507334, LOC440895, MALL, MIR4436B1, MIR4436B2, NPHP1, RGPD5, RGPD6
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257946
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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