A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173801



Internal ID15530969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25778482..25891593hg38UCSC Ensembl
Innerchr1:26104973..26218084hg19UCSC Ensembl
Innerchr1:25977560..26090671hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38113112
hg19113112
hg18113112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545883
Supporting Variants
SamplesHGDP01023
Known GenesAUNIP, LOC646471, MAN1C1, MTFR1L, PAQR7, SEPN1, STMN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173801
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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