A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730219



Internal ID21401030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6198014..9936872hg38UCSC Ensembl
chrY:6066055..9774481hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg383738859
hg193708427
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258243, nssv16257656, nssv16257909, nssv16256963
SamplesHG00512, NA19239
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)nsv4730219
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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