A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181534



Internal ID21320330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72064898..72065202hg38UCSC Ensembl
chr10:73824656..73824960hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3942870
Supporting Variants
SamplesHG002
Known GenesSPOCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181534
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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