A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730264



Internal ID21401075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97436188..97461596hg38UCSC Ensembl
chr7:97065500..97090908hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3825409
hg1925409
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257364, nssv16256829, nssv16258327, nssv16258019, nssv16256945, nssv16257075, nssv16256818, nssv16256049
SamplesHG00731, HG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730264
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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