A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526935



Internal ID22396319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7642949..7643210hg38UCSC Ensembl
chr1:7703009..7703270hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14311116, nssv14311115
SamplesNA19238, NA19240
Known GenesCAMTA1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526935
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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