A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973961



Internal ID22748896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88078611..88555937hg38UCSC Ensembl
chr7:87707926..88185252hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38477327
hg19477327
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435252
Samples
Known GenesADAM22, SRI, STEAP4
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973961
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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