A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730052



Internal ID21400868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:16254055..16322813hg38UCSC Ensembl
chrY:18365935..18434693hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3868759
hg1968759
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258103, nssv16258028, nssv16257295, nssv16256161
SamplesHG00512, NA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730052
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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