A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256963



Internal ID21400186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6240762..9910296hg38UCSC Ensembl
chrY:6108803..9747905hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg383669535
hg193639103
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730219
Supporting Variants
SamplesNA19239
Known GenesAMELY, FAM197Y2, FAM197Y5, PRKY, RBMY1A3P, RBMY3AP, TBL1Y, TSPY1, TSPY10, TSPY2, TSPY3, TSPY4, TSPY8, TTTY1, TTTY11, TTTY12, TTTY16, TTTY18, TTTY19, TTTY1B, TTTY2, TTTY20, TTTY21, TTTY21B, TTTY22, TTTY23, TTTY23B, TTTY2B, TTTY7, TTTY7B, TTTY8, TTTY8B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256963
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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