A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497362



Internal ID22555296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52951494..52952493hg38UCSC Ensembl
chr5:52247324..52248323hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842466
Supporting Variants
Samples
Known GenesITGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497362
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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