A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730076



Internal ID21400892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52879830..52977241hg38UCSC Ensembl
chrX:52908860..53006423hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3897412
hg1997564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258139, nssv16257486, nssv16257797, nssv16257729, nssv16258480, nssv16257205, nssv16256530, nssv16258306, nssv16257319, nssv16257160, nssv16257543, nssv16256157, nssv16258393, nssv16256897, nssv16257108, nssv16256770, nssv16256280, nssv16257276, nssv16258606, nssv16258423, nssv16257032, nssv16256137, nssv16256010, nssv16258013, nssv16256987, nssv16256190, nssv16257724, nssv16256991, nssv16257880, nssv16257498, nssv16256287, nssv16256757, nssv16258568, nssv16256169, nssv16258603, nssv16257554
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesFAM156A, FAM156B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730076
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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