A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998648



Internal ID16944914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:157768609..157861008hg38UCSC Ensembl
Outerchr7:157561301..157653700hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3892400
hg1992400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951671
Supporting Variants
SamplesBILGI_BIOE
Known GenesLOC100506585, PTPRN2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998648
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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