A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715629



Internal ID139295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81945298..82544214hg38UCSC Ensembl
chr17:79903174..80502090hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38598917
hg19598917
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556495
Supporting Variants
Samples
Known GenesASPSCR1, C17orf62, CCDC57, CD7, CSNK1D, DCXR, DUS1L, FASN, FOXK2, GPS1, HEXDC, LRRC45, MIR6787, MYADML2, NARF, NOTUM, OGFOD3, RAC3, RFNG, SECTM1, SLC16A3, STRA13, TEX19, UTS2R
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715629
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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