A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997097



Internal ID16943363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24339811..24352410hg38UCSC Ensembl
Outerchr1:24666301..24678900hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3812600
hg1912600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950302
Supporting Variants
SamplesBILGI_BIOE
Known GenesGRHL3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997097
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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