A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711187



Internal ID134853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7200945..7654512hg38UCSC Ensembl
chr17:7104264..7557830hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38453568
hg19453567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518154
Supporting Variants
Samples
Known GenesACADVL, ACAP1, ATP1B2, C17orf74, CD68, CHRNB1, CLDN7, CTDNEP1, DLG4, DVL2, EIF4A1, EIF5A, ELP5, FGF11, FXR2, GABARAP, GPS2, KCTD11, MIR324, MPDU1, NEURL4, NLGN2, PHF23, PLSCR3, POLR2A, SAT2, SENP3, SENP3-EIF4A1, SHBG, SLC2A4, SLC35G6, SNORA48, SNORA67, SNORD10, SOX15, SPEM1, TMEM102, TMEM256, TMEM256-PLSCR3, TMEM95, TNFSF12, TNFSF12-TNFSF13, TNFSF13, TNK1, YBX2, ZBTB4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711187
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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