A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124244



Internal ID19264014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98393046..98393140hg38UCSC Ensembl
Outerchr7:98022358..98022452hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958316, nssv3992325
SamplesKWS2, KWS1
Known GenesBAIAP2L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124244
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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