A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137304



Internal ID19268286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:149017591..149017679hg38UCSC Ensembl
Outerchr7:148714683..148714771hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975588, nssv3958356
SamplesKWS2, KWS1
Known GenesPDIA4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137304
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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