A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730168



Internal ID21400979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50078203..50425115hg38UCSC Ensembl
chr11:50039361..50384286hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38346913
hg19344926
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258314, nssv16255963, nssv16255937, nssv16257751, nssv16257332, nssv16258110, nssv16256285, nssv16255961, nssv16258255, nssv16257225, nssv16257557, nssv16255843, nssv16258456, nssv16255898, nssv16255853, nssv16256407, nssv16256233, nssv16257465, nssv16257306, nssv16256462, nssv16256086, nssv16258091, nssv16256702, nssv16257539, nssv16258622, nssv16258656, nssv16258785, nssv16258415
SamplesHG00512, NA19238, HG00731, HG00732, HG00733, HG00513, HG00514
Known GenesLOC441601, LOC646813
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730168
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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