A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730130



Internal ID21400941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51669469..51727337hg38UCSC Ensembl
chrX:51412401..51470433hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3857869
hg1958033
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258517, nssv16258705, nssv16256864, nssv16255860, nssv16258754, nssv16257104, nssv16257841, nssv16256574, nssv16258579, nssv16258810, nssv16258545, nssv16258196, nssv16255935, nssv16258651, nssv16257658, nssv16258634, nssv16258661, nssv16258022, nssv16257624, nssv16256483, nssv16256975, nssv16258686, nssv16258117, nssv16256295, nssv16258155, nssv16258353, nssv16256705, nssv16257143, nssv16258858, nssv16257973, nssv16256189, nssv16258873
SamplesHG00512, NA19238, NA19239, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesCENPVP1, CENPVP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730130
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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