A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15197629



Internal ID21336425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35136429..35137030hg38UCSC Ensembl
chr6:35104206..35104807hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953731
Supporting Variants
SamplesHG002
Known GenesTCP11
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15197629
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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