A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997048



Internal ID16943314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137607249..137625148hg38UCSC Ensembl
Outerchr9:140501701..140519600hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3817900
hg1917900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951212
Supporting Variants
SamplesBILGI_BIOE
Known GenesARRDC1, C9orf37, EHMT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997048
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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