A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370989



Internal ID22596658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15758291..16862696hg38UCSC Ensembl
chr17:15661605..16766010hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381104406
hg191104406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940764
Supporting Variants
Samples
Known GenesADORA2B, CCDC144A, CDRT15P2, CENPV, FAM106CP, FAM211A, FAM211A-AS1, KRT16P2, MEIS3P1, MIR1288, NCOR1, PIGL, SNORD49A, SNORD49B, SNORD65, TRPV2, TTC19, UBB, USP32P1, ZNF287, ZNF624, ZSWIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370989
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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