A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482485



Internal ID22540390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:935164..964006hg38UCSC Ensembl
chr1:870544..899386hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3828843
hg1928843
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830546
Supporting Variants
Samples
Known GenesKLHL17, NOC2L, SAMD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482485
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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