A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035588



Internal ID20602628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32802650..32843828hg38UCSC Ensembl
chr17:31129668..31170846hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3841179
hg1941179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500888
Supporting Variants
Samples
Known GenesMYO1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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