A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137257



Internal ID19271374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:75664086..75664165hg38UCSC Ensembl
Outerchr7:75293404..75293483hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975539, nssv3958302
SamplesKWS2, KWS1
Known GenesHIP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137257
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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