A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277968



Internal ID20487186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7004307..7004359hg38UCSC Ensembl
chr17:6907626..6907678hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734515
Supporting Variants
Samples
Known GenesALOX12, LOC100506713
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277968
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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