A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031994



Internal ID19121216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111340277..111683497hg38UCSC Ensembl
Innerchr7:110980333..111323553hg19UCSC Ensembl
Innerchr7:110767569..111110789hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38343221
hg19343221
hg18343221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6573n100
Supporting Variantsnssv3645261
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031994
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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